Bacterium

ABSTRACT

The present invention relates in one aspect to a fast acidifying lactic acid bacterium that generates a viscosity in fermented milk greater than about 62 Pa·s after 14 days of storage at 6° C.

FIELD OF INVENTION

The present invention relates to inter alia a fast acidifying lacticacid bacterium with improved texturzing properties.

BACKGROUND TO THE INVENTION

The food industry uses bacteria in order to improve the taste and thetexture of foods and also to extend the shelf life of these foods. Inthe case of the dairy industry, lactic bacteria are commonly used inorder to, for example, bring about the acidification of milk (byfermentation) and to texturize the product into which they areincorporated. Among the lactic bacteria commonly used in the foodindustry, examples include the genera Streptococcus, Lactococcus,Lactobacillus, Leuconostoc, Pediococcus and Bifidobacterium.

The lactic acid bacteria of the species Streptococcus thermophilus areused extensively alone or in combination with other bacteria for theproduction of food products, in particular fermented products. They areused in particular in the formulation of the ferments used for theproduction of fermented milks, for example yogurts. Certain bacteriaplay a dominant role in the development of the texture of the fermentedproduct. This characteristic is closely linked to the production ofpolysaccharides. Among the strains of Streptococcus thermophilus it ispossible to distinguish texturizing and non-texturizing strains.

In addition, cultures—such as starter cultures—are used extensively inthe food industry in the manufacture of fermented products includingmilk products (such as yoghurt, butter and cheese), meat products,bakery products, wine and vegetable products. The preparation ofcultures is labour intensive, occupying much space and equipment, andthere is a considerable risk of contamination with spoilage bacteriaand/or phages during the step of propagation. The failure of bacterialcultures by bacteriophage (phage) infection and multiplication is amajor problem with the industrial use of bacterial cultures. There aremany different types of phages with varying mechanisms to attackbacteria. Moreover, new strains of bacteriophages appear.

Strategies used in industry to minimise bacteriophage infection, andthus failure of a bacterial culture, include the use of: (i) mixedstarter cultures; and (ii) the alternate use of strains having differentphage susceptibility profiles (strain rotation).

(i) Traditionally, starter cultures in the dairy industry are mixturesof lactic acid bacterial strains. The complex composition of mixedstarter cultures ensures that a certain level of resistance to phageattack is present. However, repeated sub-culturing of mixed straincultures leads to unpredictable changes in the distribution ofindividual strains and eventually undesired strain dominance. This inturn may lead to increased susceptibility to phage attack and risk offermentation failures.

(ii) The rotation of selected bacterial strains which are sensitive todifferent phages is another approach to limit phage development.However, it is difficult and cumbersome to identify and select asufficient number of strains having different phage type profiles toprovide an efficient and reliable rotation program. In addition, thecontinuous use of strains requires careful monitoring for new infectiousphages and the need to quickly substitute a strain which is infected bythe new bacteriophage by a resistant strain. In manufacturing plantswhere large quantities of bulk starter cultures are made ahead of time,such a quick response is usually not possible.

There is a continuing need in the art to provide improved bacterialstrains for use in the food/feed industry—such as bacterial strains thathave improved texturizing properties. Improved bacterial strains thatare phage resistant are particularly desirable.

SUMMARY OF THE PRESENT INVENTION

The fast acidifying lactic acid bacterium described herein has numerousadvantages. By way of example, the fast acidifying lactic acid bacteriumhas advantages in terms of texturizing the media into which it isincorporated. By way of further example, it makes it possible to obtaingels from, for example, fermented milks, which are thick, sticky,coated, stringy, resistant to stirring and/or not granular.

Advantageously, the fast acidifying lactic acid bacterium isbacteriophage resistant thereby minimising bacteriophage infection, andthus failure of the bacterial culture. This is an important property ofthe lactic acid bacterium described herein because it reduces the riskof phage incidents during production, which may stop production for aperiod of time for decontamination.

Most advantageously, the fast acidifying lactic acid bacterium describedherein has advantageous texturizing properties and is also phageresistant.

SUMMARY ASPECTS OF THE PRESENT INVENTION

Aspects of the present invention are presented in the accompanyingclaims.

In a first aspect, there is provided a fast acidifying lactic acidbacterium that generates a viscosity in fermented milk greater thanabout 62 Pa·s.

In a particularly preferred aspect, there is provided a fast acidifyinglactic acid bacterium that generates a viscosity in fermented milkgreater than about 62 Pa·s and which bacterium is phage resistant.

In another aspect, there is provided a lactic acid bacterium comprisingthe sequence set forth in SEQ ID No. 19 or a homologue thereof with atleast 75% identity thereto.

In a further aspect, there is provided an isolated Streptococcusthermophilus strain deposited under the Budapest Treaty by DaniscoDeutschland Niebüll GmbH, Buch-Johannsen Strasse.1, Niebüll-D-25899,Germany at DSMZ (Deutsche Sammlung von Mikroorganismen und ZellkulturenGmbH, Mascheroder Weg 1 b, D-38124 Braunschweig) under deposit number18344 on 14 Jun. 2006. We hereby confirm that the depositor hasauthorised the applicant to refer to the deposited biological materialin this application and has given his unreserved and irrevocable consentto the deposited material being made available to the public.

There is also provided a cell culture comprising the lactic acidbacterium or the strain described herein.

In a further aspect, there is provided a food, food additive, feed,nutritional supplement, or probiotic supplement comprising the lacticacid bacterium, the strain, or the cell culture as described herein.

A method for preparing a food, food additive, feed, nutritionalsupplement, or probiotic supplement comprising the step of adding thelactic acid bacterium, the strain, or the cell culture to said food,food additive, feed, nutritional supplement, or probiotic supplement.

In a further aspect, a food, food additive, feed, nutritionalsupplement, or probiotic supplement obtained or obtainable by the methoddescribed herein. There is also described the use of the lactic acidbacterium, the strain, or the cell culture for preparing a food, foodadditive, feed, nutritional supplement, or probiotic supplement.

In a further aspect, we described a method for modifying the viscosityof a food, food additive, feed, nutritional supplement, or probioticsupplement, comprising adding the lactic acid bacterium, the strain, orthe cell culture to said, food, food additive, feed, nutritionalsupplement, or probiotic supplement.

A food, food additive, feed, nutritional supplement, or probioticsupplement obtained or obtainable by the method is also provided.

There is provided, in a further aspect, the use of the lactic acidbacterium, the strain, or the cell culture for modifying the viscosityof a food, food additive, feed, nutritional supplement, or probioticsupplement.

A method is also described for identifying a bacterium belonging to thegenus Streptococcus comprising the step of screening the bacterium forthe sequence set forth in SEQ ID No. 19 or a homologue thereof with atleast 75% identity thereto.

A method for identifying a bacterium belonging to the genusStreptococcus is also described comprising the step of amplifying theCRISPR locus of a bacterium using at least one forward and at least onereverse oligonucleotide primer, wherein each of the primers flankopposite sides of one or more CRISPR spacers that are absent inStreptococcus thermophilus DSMZ-18344.

A bacterium belonging to the genus Streptococcus that is identified oridentifiable by the method is also provided in a further aspect.

In another aspect, there is described a nucleotide sequence comprisingthe sequence set forth in SEQ ID No. 19 or a homologue thereof with atleast 75% identity thereto.

A nucleotide sequence complementary to the nucleotide sequence is alsoprovided, as is a construct or a vector comprising the nucleotidesequence

In a further aspect, there is described a host cell comprising theconstruct or the vector.

An oligonucleotide primer that is capable of hybridising to thenucleotide sequence is also provided.

In still a further aspect, the use of the oligonucleotide primer foridentifying a bacterium belonging to the genus Streptococcus isdescribed.

There is also provided a lactic acid bacterium, an isolated culture, acell culture, a food, food additive, feed, nutritional supplement,probiotic supplement, a method, a use, a nucleic acid sequence, aconstruct, a vector, a host cell, an amino acid sequence, or anoligonucleotide primer as hereinbefore described with reference to theaccompanying description and figures.

Other aspects of the present invention are presented in the accompanyingclaims and in the following description and discussion. These aspectsare presented under separate section headings. However, it is to beunderstood that the teachings under each section heading are notnecessarily limited to that particular section heading.

PREFERRED EMBODIMENTS

Preferably, the bacterium is phage resistant.

Preferably, the bacterium is selected from the group consisting ofStreptococcus, Lactococcus, Lactobacillus, Leuconostoc, Pediococcus andBifidobacterium. Preferably, the bacterium is Streptococcusthermophilus.

Preferably, the Streptococcus thermophilus belongs to the geneticcluster CL0189. Preferably, the lactic acid bacterium comprises thesequence set forth in SEQ ID No. 20.

Preferably, the cell culture is a starter culture, a probiotic cultureor a dietary supplement.

Preferably, the culture comprises one or more further lactic acidbacteria selected from the genera consisting of Streptococcus,Lactococcus, Lactobacillus, Leuconostoc, Pediococcus andBifidobacterium.

Preferably, the culture comprises one or more further lactic acidbacteria selected from the species consisting of Lactobacillusdelbrueckii subsp. bulgaricus, Lactobacillus acidophilus, Lactobacilluscasei and/or Bifidobacterium.

Preferably, the food, food additive, feed, nutritional supplement, orprobiotic supplement is a dairy, meat or cereal food, food additive,feed, nutritional supplement, or probiotic supplement

Preferably, the dairy food, food additive, feed, nutritional supplement,or probiotic supplement is a fermented milk, yoghurt, cream, maturedcream, cheese, fromage frais, a milk beverage, a processed cheese, acream dessert, a cottage cheese or infant milk.

Preferably, the milk comprises milk of animal and/or plant origin.

Preferably, the food, food additive, feed, nutritional supplement, orprobiotic supplement comprises or consists of a fermented food, foodadditive, feed, nutritional supplement, or probiotic supplement.

Preferably, the food, food additive, feed, nutritional supplement, orprobiotic supplement comprises or consists of a dairy food, foodadditive, feed, nutritional supplement, or probiotic supplement.

Preferably, the forward oligonucleotide primer hybridises to SEQ ID No.1 and the reverse oligonucleotide primer hybridises to any of SEQ ID No.2, SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, SEQ ID No. 7,SEQ ID No. 8, SEQ ID No. 9, SEQ ID No. 10, SEQ ID No. 11, SEQ ID No. 12,SEQ ID No. 13, SEQ ID No. 14, SEQ ID No. 15, SEQ ID No. 16 and/or SEQ IDNo. 17.

Preferably, the forward oligonucleotide primer hybridises to any of SEQID No. 2, SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, SEQ IDNo. 7 and/or SEQ ID No. 8 and a reverse oligonucleotide primerhybridises to any of SEQ ID No. 9, SEQ ID No. 10, SEQ ID No. 11, SEQ IDNo. 12, SEQ ID No. 13, SEQ ID No. 14, SEQ ID No. 15, SEQ ID No. 16and/or SEQ ID No. 17.

Preferably, the forward oligonucleotide primer hybridises to any of SEQID No. 2, SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, SEQ IDNo. 7 and/or SEQ ID No. 8 and the reverse oligonucleotide primerhybridises to SEQ ID No. 18.

Preferably, the forward oligonucleotide primer hybridises to any of SEQID No. 9, SEQ ID No. 10, SEQ ID No. 11, SEQ ID No. 12, SEQ ID No. 13,SEQ ID No. 14, SEQ ID No. 15, SEQ ID No. 16 and/or SEQ ID No. 17 and thereverse oligonucleotide primer hybridises to SEQ ID No. 18.

Preferably, the bacterium belonging to the genus Streptococcus isStreptococcus thermophilus.

Preferably, the Streptococcus thermophilus strain belongs to the geneticcluster CL0189.

Preferably, the Streptococcus thermophilus strain has substantially thesame characteristics as the Streptococcus thermophilus strain depositedat DSMZ (Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH,Mascheroder Weg 1 b, D-38124 Braunschweig) under deposit number 18344 on14 Jun. 2006.

Preferably, the Streptococcus thermophilus strain is the same as theStreptococcus thermophilus strain deposited DSMZ (Deutsche Sammlung vonMikroorganismen und Zellkulturen GmbH, Mascheroder Weg 1 b, D-38124Braunschweig) under deposit number 18344 on 14 Jun. 2006.

The term “fast acidifying strain” as used herein preferably means astrain that has the following properties: a speed of acidification ofless than −0.0100 upH/min and a time to reach pH 4.6 of less than 540minutes at 43° C. when the inoculation rate is between 1E6 cfu/ml and1E7 cfu/ml of milk (following the fermentated milk process described inthe section entitled “Fermented Milk Process” below).

FIGURES

FIG. 1

Comparison of the results obtained using EPSAD PCR-RFLP for S.thermophilus CNCM I-2423, S. thermophilus CNCM I-2425 and S.thermophilus DSMZ-18344.

FIG. 2

Organisation of S. thermophilus eps gene clusters. All known eps operonsconsist of a common proximal part (epsA-B-C-D genes) which is followedby a highly variable part.

FIG. 3

Schematic representation of the sequence of the spacers of the CRISPR 1locus of S. thermophilus DSMZ-18344, S. thermophilus CNCM I-2425, S.thermophilus CNRZ385 and S. thermophilus CNCM I-2423. Each squarerepresents one spacer sequence.

DETAILED DESCRIPTION OF THE INVENTION Lactic Acid Bacteria

As used herein the term “lactic acid bacteria” refers to Gram positive,microaerophillic or anaerobic bacteria which ferment sugar with theproduction of acids including lactic acid as the predominantly producedacid, acetic acid, formic acid and propionic acid. They belong to thetaxonomic group of the Firmicutes. Devoid of catalase, the lacticbacteria constitute a heterogeneous group of bacteria in the form ofcocci for the genera Aeroccus, Enterococcus, Lactococcus, Leuconostoc,Oenococcus, Pediococcus, Streptococcus, Tetragenococcus, Vagococcus andWeissella, or in the form of rods for the genera Lactobacillus andCarnobacterium.

The industrially most useful lactic acid bacteria are found among thegenera Lactococcus, Lactobacillus, Bifidobacterium, Streptococcus,Leuconostoc, Pediococcus and Propionibacterium. In one embodiment, it istherefore preferred that the lactic acid bacterium is selected from thisgroup of genera.

In a particularly preferred embodiment, the lactic acid bacteriumbelongs to the genus Streptococcus.

A preferred species of lactic bacterium is Streptococcus thermophilus.Preferably, the Streptococcus thermophilus belongs to the geneticcluster CL0189. Streptococcus thermophilus is a species naturallypresent in milk and widely used in the food, and in particular dairyindustry because it can be used to acidify and texturise products—suchas milk. It is a homofermentative thermophilic bacterium.

As described in further detail herein, lactic acid bacteria startercultures are commonly used in the food industry as mixed strain culturescomprising one or more species. Mixtures of preferred strains includemixtures of the lactic acid bacterium described herein with one or moreStreptococcus strains—such as different Streptococcus thermophilusstrains—or with one or more strains belonging to the genera Lactococcus,Lactobacillus, Bifidobacterium, Streptococcus, Leuconostoc, Pediococcusand/or Propionibacterium.

Mixtures of the lactic acid bacterium described herein withLactobacillus delbrueckii subsp. Bulgaricus, Lactobacillus acidophilus,Lactobacillus casei, Lactococcus lactis and/or Bifidobacterium arepreferred.

Mixtures of the lactic acid bacterium described herein withLactobacillus delbrueckii subsp. bulgaricus are particularly preferred.Such mixed strain cultures are typically used as yoghurt startercultures where a symbiotic relationship exists between the species(Rajagopal et al. J. Dairy Sci., 73, p. 894-899, 1990).

The lactic acid bacteria and mixtures thereof may be used in thecultures described herein.

In one aspect, there is provided a fast acidifying lactic acid bacteriumthat generates a viscosity in fermented milk greater than about 62 Pa·s.

In addition an increase in the rate of acidification also reduces therisk of fermentation failure due to phage infection.

Preferably, said bacterium comprises the sequence set forth in SEQ IDNo. 19 or a homologue thereof with at least 75% identity thereto.

Preferably, said bacterium comprises the sequence set forth in SEQ IDNo. 20 or a variant, fragment, homologue or derivative thereof.

In a further aspect, there is provided a lactic acid bacteriumcomprising the sequence set forth in SEQ ID No. 19 or a homologuethereof with at least 75% identity thereto.

In a further aspect, there is provided a lactic acid bacteriumcomprising the sequence set forth in SEQ ID No. 20 or a variant,fragment, homologue or derivative thereof.

In a particularly preferred aspect, the present invention relates to astrain of Streptococcus thermophilus deposited at DSMZ (DeutscheSammlung von Mikroorganismen und Zellkulturen GmbH, Mascheroder Weg 1 b,D-38124 Braunschweig) under deposit number 18344 on 14 Jun. 2006.

The lactic acid bacterium may be a mutant and/or a variant of the lacticacid bacterium described herein. Preferably, this mutant and/or variantlactic acid bacterium has one or more (preferably, all) of thecharacteristics of the S. thermophilus strain of the present inventione.g. the mutant and/or variant lactic acid bacterium is a fastacidifying lactic acid bacterium; and/or the mutant and/or variantlactic acid bacterium generates a viscosity in fermented milk greaterthan about 62 Pa·s, preferably about 68 Pa·s; and/or the mutant and/orvariant lactic acid bacterium is phage resistant; and/or the mutantand/or variant lactic acid bacterium belongs to the genetic clusterCL0189; and/or the mutant and/or variant lactic acid bacterium comprisesthe sequence set forth in SEQ ID No. 20; and/or the mutant and/orvariant lactic acid bacterium comprises the sequence set forth in SEQ IDNo. 19 or a variant, fragment, homologue or derivative thereof.

Acidifying Activity

Acidifying activity is typically characterised by three parameters: thekinetics of acidification, the titratable acidity and the finalfermentation pH which determines the organoleptic characteristics of theproduct and its preservation quality, and the post-acidification whichdevelops during preservation of the product.

Advantageously, a high rate of acidification makes it possible to reducethe period during which a product is sensitive to contaminants (pH>4.7)and thereby to reduce the risk of bacterial contamination. An increasein the rate of acidification also enhances the economics of the processby increasing the productivity and the flexibility of the industrialmaterial.

The acidifying activity of lactic acid bacteria may be determined usingvarious methods that are known in the art. By way of example, the lacticacid bacteria may be initially grown in broth and then in sterilereconstituted skimmed milk supplemented with yeast extract and glucosefor two successive subcultures. Sterile reconstituted skimmed milk isthen inoculated with a 24-h activated culture and pH changes determinedusing pH meters during incubation.

Advantageously, the lactic acid bacterium according to the presentinvention is fast acidifying since it can be characterised by a fastacidification of milk during the fermentation process.

Preferably, the speed of acidification is from about −0.013 upH/min toabout −0.019 upH/min. More preferably, the speed of acidification isfrom about −0.0135 upH/min to about −0.018 upH/min. More preferably, thespeed of acidification is from about −0.014 upH/min to about −0.017upH/min. More preferably, the speed of acidification is from about−0.0145 upH/min to about −0.017 upH/min. More preferably, the speed ofacidification is from about −0.015 upH/min to about −0.017 upH/min. Morepreferably, the speed of acidification is from about −0.015 upH/min toabout −0.017 upH/min. Most preferably the speed of acidification isabout −0.0169 upH/min.

This rate of acidification compares favourably to other fast acidifyingstrains of bacteria—such as 0.0129 upH/min, 0.0167 upH/min and 0.0209upH/min for S. thermophilus CNCM 1-2423, S. thermophilus CNCM I-2980 andS. thermophilus CNCM I-2425, respectively.

S. thermophilus CNCM I-2423 has been previously deposited at the CNCM asdeposit number I-2423 and is described in WO2004/085607.

S. thermophilus CNCM I-2425 has been previously deposited at the CNCM asdeposit number 1-2425

S. thermophilus CNCM I-2980 has been previously deposited at the CNCM asdeposit number 1-2980 and is described in WO2004/085607.

Fast acidifying S. thermophilus is a bacterium that is typically able tocoagulate milk in less than 540 min at 43° C.+/−1° C. when theinoculation rate is between 1E6 cfu/ml and 1E7 cfu/ml of milk. Themaximum speed of acidification is the maximum value of the derived curvepH versus time. This final measurement may be obtained using on line pHmeasurement in milk using a CINAC device (Ysebaert Ltd).

In one embodiment, the rate of acidification is measured using methodsthat are commonly known in the art. Typically, the rate of acidificationwill be measured by monitoring the change in pH over time.

In another embodiment, the rate of acidification is measured using aCINAC device which is an extensively used apparatus in the dairyindustry to analyse acidification properties of lactic acid bacteria.

An automated system for measuring the rate of acidification is wellknown to the person of ordinary skill in the art. Reference can be foundin (for example) FR 2 629 612 for example. The CINAC automated system istaught in the article Corrieu, G. et al Process (ISSN 0998-6650); 1992,No. 1068, pp 24-27 (10 ref.).

Texturizing/Viscosity

As described herein, a lactic acid bacterium with improved texturizingproperties or activities is provided. In particular, the lactic acidbacterium exhibits the property of conferring viscosity to afermentation medium.

The lactic acid bacterium generates fermented milk having a viscositygreater than about 62 Pa·s, more preferably greater than about 65 Pa·s,more preferably greater than about 68 Pa·s.

Preferably, the lactic acid bacterium generates fermented milk having aviscosity in the range of about 62 Pa·s to about 75 Pa·s, preferablyfrom about 65 Pa·s to about 75 Pa·s, more preferably from about 62 Pa·sto about 68 Pa·s, most preferably from about 65 to about 68 Pa·s, morepreferably about 68 Pa·s.

Preferably, the viscosity is measured after 14 days of storage at about6° C.

The lactic acid bacteria described herein are strongly texturizing.

In one embodiment, the lactic acid bacterium generates fermented milkhaving the viscosity described herein as measured using the one or moreof the methods described below.

Various rheological measurements are known in the art—such as flow andviscosity.

Fermented Milk Process

In one embodiment, fresh fermented milks are produced at lab scale. Themilk base is composed of commercial UHT milk supplemented with 3% (w/w)semi-skimmed milk powder. After mixing, the milk base is heated during10 min+/−1 min at 90° C.+/−0.2° C. The base is then cooled down at 43°C.+/−1° C. in a water bath regulated at 43° C.+/−1° C. and the milk isdispatched into 125 ml glass beakers. The milk is inoculated with thebacterium at a ratio of 1E6-1E7 cfu/ml. The fermentation is carried outat 43° C.+/−1° C. without stirring and it is stopped when the pH reaches4.6+/−0.05. At this moment, the fresh fermented milk is quickly cooleddown at 6° C.+/−1° C. in less than 1 hour. Finally, the products arestored at this temperature during 28 days.

Method to Measure Viscosity:

In one embodiment, the viscosity measurements are carried out at 6° C.on fermented milks, after storage for 1, 7, 14 and 28 days at 6° C. Theapparatus used is an RVFtype Brookfield® viscometer (BrookfieldEngineering Laboratories, Inc.) mounted on a Helipath stand (BrookfieldEngineering Laboratories, Inc.) The viscometer is equipped with a type Cneedle and the oscillation speed applied to the needle is 10 rpm. Inaccordance with the present invention this method is a preferred methodfor measuring viscosity.

Method to Measure Flow:

In another embodiment, the flow measurements are carried out at 6° C. onfermented milks, after storage for 14 days at 6° C. and which have beenpreviously stirred. The apparatus used is an ARI000-N rheometer (TAInstruments) equipped with co-axial cylinders (Radius 1=15 mm, Radius2=13.83 mm, Height 32 mm, Air gap=2 mm). For the ascending segment shearstress [Pa] is applied in a continuous sweep from 0 to 60 Pa for aduration of 1 minute according to a linear mode. For the descendingsegment, the shear stress [Pa] applied in a continuous sweep varies from60 to 0 Pa for a duration of 1 minute according to a linear mode. Thevalues taken into account are the thixotropic area (Pa/s) and the yieldstress (Pa); the latter is calculated according to the Casson model.

In accordance with the present invention, the viscosity of a food, foodadditive, feed, nutritional supplement, or probiotic supplement may bemodified or modulated using the lactic acid bacterium described herein.Preferably, the viscosity is increased.

Bacteriophage

As used herein, the term “bacteriophage” has its conventional meaning asunderstood in the art ie. a virus that selectively infects one or morebacteria. Many bacteriophages are specific to a particular genus orspecies or strain of bacteria.

The term “bacteriophage” is synonymous with the term “phage”.

The bacteriophage may be a lytic bacteriophage or a lysogenicbacteriophage.

A lytic bacteriophage is one that follows the lytic pathway throughcompletion of the lytic cycle, rather than entering the lysogenicpathway. A lytic bacteriophage undergoes viral replication leading tolysis of the cell membrane, destruction of the cell, and release ofprogeny bacteriophage particles capable of infecting other cells.

A lysogenic bacteriophage is one capable of entering the lysogenicpathway, in which the bacteriophage becomes a dormant, passive part ofthe cell's genome through prior to completion of its lytic cycle.

Bacteriophages may include, but are not limited to, bacteriophages thatbelong to any of the following virus families: Corticoviridae,Cystoviridae, Inoviridae, Leviviridae, Microviridae, Myoviridae,Podoviridae, Siphoviridae, or Tectiviridae.

Advantageously, the lactic acid bacterium according to the presentinvention is phage resistant.

Over the last 2 decades a library of more than one thousand phagesvirulent for industrial S. thermophilus strains have been collated. Thiscollection of phages was intensively studied and their host spectrum wasestablished. This allowed the identification of a set of 60 phagesrepresentative of all the host spectrums identified within thecollection of phages. Each of these representative phages was tested onstrains DSMZ18344, CNCM I-2423 and CNCM I-2425, as described herein.CNCM I-2423 was found to be sensitive to phage D4126 and D3215. StrainCNCMI-2425 was found to be sensitive to phage D4369. On the contrarystrain DSMZ-18344 of the present invention was resistant to all therepresentative phages tested.

In one embodiment, the lactic acid bacterium of the present invention isresistant to phage D4126 and/or D3215 and/or phage D4369.

In one embodiment, the lactic acid bacterium according to the presentinvention is resistant to one or more bacteriophage or one or more setsof bacteriophage. In another embodiment, the lactic acid bacteriumaccording to the present invention is resistant to the samebacteriophage that strain CNCM I-2423 and/or CNCM I-2425 are resistantto.

CRISPR Locus

As used herein, the term “CRISPR locus” is defined as the DNA segmentwhich includes all of the CRISPR repeats, starting with the firstnucleotide of the first CRISPR repeat and ending with the lastnucleotide of the last (terminal) CRISPR repeat.

The CRISPR locus is a distinct class of interspersed short sequencerepeats (SSRs) that were first recognized in E. coli (Ishino et al.(1987) J. Bacteriol. 169:5429-5433; Nakata et al. (1989) J. Bacteriol.171:3553-3556). Similar interspersed SSRs have been identified inHaloferax mediterranei, Streptococcus pyogenes, Anabaena, andMycobacterium tuberculosis (Groenen et al. (1993) Mol. Microbiol.10:1057-1065; Hoe et al. (1999) Emerg Infect. Dis. 5:254-263; Masepohlet al. (1996) Biochim. Biophys. Acta 1307:26-30; Mojica et al. (1995)Mol. Microbiol. 17:85-93). The CRISPR loci differ from other SSRs by thestructure of the repeats, which have been termed short regularly spacedrepeats (SRSRs) (Janssen et al. (2002) OMICS J. Integ. Biol. 6:23-33;Mojica et al. (2000) Mol. Microbiol. 36:244-246). The repeats are shortelements that occur in clusters, that are always regularly spaced byunique intervening sequences with a constant length (Mojica et al.(2000) Mol. Microbiol. 36:244-246). Although the repeat sequences arehighly conserved between strains, the number of interspersed repeats andthe sequences of the spacer regions differ from strain to strain (vanEmbden et al. (2000) J. Bacteriol. 182:2393-2401).

The common structural characteristics of the CRISPR locus are describedin Jansen et al. (2002) as (i) the presence of multiple short directrepeats, which show no or very little sequence variation within a givenlocus; (ii) the presence of non-repetitive spacer sequences between therepeats of similar size; (iii) the presence of a common leader sequenceof a few hundred basepairs in most species harbouring multiple CRISPRloci; (iv) the absence of long open reading frames within the locus; and(v) the presence of one or more cas genes.

CRISPR repeats are typically short partially palindromic sequences of24-40 bp containing inner and terminal inverted repeats of up to 11 bp.Although isolated elements have been detected, they are generallyarranged in clusters (up to about 20 or more per genome) of repeatedunits spaced by unique intervening 20-58 bp sequences. CRISPR repeatsare generally homogenous within a given genome with most of them beingidentical. However, there are examples of heterogeneity in, for example,the Archaea (Mojica et al. 2000).

Advantageously, the CRISPR locus can be used to type and/or screenbacteria.

As will be appreciated by a person skilled in the art, there arenumerous different methods for screening/typing a bacterium. In thisregard, numerous methods are set forth in, for example, J. Sambrook, E.F. Fritsch, and T. Maniatis, 1989, Molecular Cloning: A LaboratoryManual, Second Edition, Books 1-3, Cold Spring Harbor Laboratory Press;Ausubel, F. M. et al. (1995 and periodic supplements; Current Protocolsin Molecular Biology, ch. 9, 13, and 16, John Wiley & Sons, New York,N.Y.); B. Roe, J. Crabtree, and A. Kahn, 1996, DNA Isolation andSequencing: Essential Techniques, John Wiley & Sons; M. J. Gait(Editor), 1984, Oligonucleotide Synthesis: A Practical Approach, IrlPress; and, D. M. J. Lilley and J. E. Dahlberg, 1992, Methods ofEnzymology: DNA Structure Part A: Synthesis and Physical Analysis of DNAMethods in Enzymology, Academic Press.

In one embodiment, amplification is used.

By “amplification” we mean the production of additional copies of anucleic acid sequence.

Amplification techniques include, but are not limited to, methodsbroadly classified as thermal cycling amplification methods andisothermal amplification methods.

Suitable thermal cycling methods include, for example, ligase chainreaction (Genomics 4:560, (1989); and Science 241: 1077 (1988)), thepolymerase chain reaction (PCR) (as described in U.S. Pat. No.4,683,195; U.S. Pat. No. 4,683,202; and U.S. Pat. No. 4,965,188) andReal time PCR; the Polymerase Ligase Chain Reaction (PCR Methods andApplic. (1991) 1:5-16); Gap-LCR (WO 90/01069); the Repair Chain Reaction(EP 439,182); and 3SR (Proc. Natl. Acad. Sci. U.S.A. (1989)86:1173-1177; Proc. Natl. Acad. Sci. U.S.A. (1990) 87:1874-1878; and WO92/0880). Isothermal amplification methods include, for example, StrandDisplacement Amplification (SDA) (Proc. Nat. Acad. Sci. USA 89:392-396(1992)), Q-beta-replicase (Bio/Technology 6:1197-1202 (1988)); nucleicacid-based Sequence Amplification (NASBA) (Bio/Technology 13:563-565(1995)); and Self-Sustained Sequence Replication (Proc. Nat. Acad. Sci.USA 87:1874-1878 (1990)).

In a preferred embodiment of the present invention, the amplificationmethod is PCR. This is generally carried out using PCR technologies wellknown in the art (Dieffenbach and Dveksler (1995) PCR Primer, aLaboratory Manual (Cold Spring Harbor Press, Plainview, N.Y.).

As is well known in the art, oligonucleotide primers can be designed foruse in amplification reactions to amplify a desired sequence.

By “primer” we mean an oligonucleotide, whether occurring naturally asin a purified restriction digest or produced synthetically, which iscapable of acting as a point of initiation of synthesis when placedunder conditions in which synthesis of a primer extension product whichis complementary to a nucleic acid strand is induced (i.e., in thepresence of nucleotides and an inducing agent—such as DNA polymerase andat a suitable temperature and pH). The primer is preferably singlestranded for maximum efficiency in amplification, but may alternativelybe double stranded. If double stranded, the primer is first treated toseparate its strands before being used to prepare extension products.Preferably, the primer is an oligodeoxyribonucleotide. The primer mustbe sufficiently long to prime the synthesis of extension products in thepresence of the inducing agent. The exact lengths of the primers willdepend on many factors, including temperature, source of primer, and theuse of the method. PCR primers are preferably at least about 10nucleotides in length (e.g. 11, 12, 13, 14, 15, 16, 17, 18 or 19nucleotides in length), and most preferably at least about 20nucleotides in length.

Methods for designing PCR primers and PCR cloning are generally known inthe art and are disclosed in Sambrook et al. (1989) Molecular Cloning: ALaboratory Manual (2d ed., Cold Spring Harbor Laboratory Press,Plainview, N.Y.). See also Innis et al., eds. (1990) PCR Protocols: AGuide to Methods and Applications (Academic Press, New York); Innis andGelfand, eds. (1995) PCR Strategies (Academic Press, New York); andInnis and Gelfand, eds. (1999) PCR Methods Manual (Academic Press, NewYork). Known methods of PCR include, but are not limited to, methodsusing paired primers, nested primers, single specific primers,degenerate primers, gene-specific primers, vector-specific primers,partially mismatched primers, and the like.

Suitably, a bacterium may be screened by amplifying (e.g. PCRamplifying) the CRISPR (e.g. CRISPR1) locus using primers targetingconserved stretches within the leader and trailer (as described inBolotin et al., (2005) Microbiology 151(8):2551-61).

Suitably, a bacterium may be screened by amplifying (e.g. PCRamplifying) selected portions of the CRISPR (e.g. CRISPR1) locus. Inthis regard, it has been surprisingly found that the Streptococcusthermophilus strain described herein lacks 5 CRISPR spacers as comparedto, for example, S. thermophilus CNCM I-2425 and S. thermophilusCNRZ385. In particular, it has been found that the Streptococcusthermophilus strain of the present invention lacks the first, second,tenth, eleventh and twelfth CRISPR1 spacers from the 5′ end of theCRISPR spacer as compared to, for example, S. thermophilus CNCM I-2425and S. thermophilus CNRZ385. As the skilled person will appreciate, thisproperty of the Streptococcus thermophilus strain of the presentinvention can advantageously be used to detect this strain sinceamplicons of different lengths will be obtained when compared to atleast S. thermophilus CNCM I-2425 and S. thermophilus CNRZ385. So forexample, a first primer could be designed to hybridise to the leadersequence at the 5′ end of the CRISPR locus and a second primer could bedesigned to hybridise downstream of the second missing CRISPR spacersequence and/or downstream of the twelfth missing CRISPR spacer in theStreptococcus thermophilus strain of the present invention. By way offurther example, a first primer could be designed to hybridisedownstream of the second missing CRISPR spacer sequence and a secondprimer could be designed to hybridise downstream of the twelfth missingspacer.

Preferably, said bacterium is screened using oligonucleotide primers,which specifically or substantially hybridise to said nucleotidesequence(s) as described herein.

In one aspect, there is provided a method for identifying aStreptococcus thermophilus strain comprising the use of anoligonucleotide primer which specifically hybridises to the sequence setforth in SEQ ID No. 19 or a homologue thereof with at least 75% identitythereto.

In a further aspect, there is provided a method for identifying aStreptococcus thermophilus strain comprising the use of oligonucleotideprimers which flank CRISPR spacers that are absent in Streptococcusthermophilus DSMZ-18344.

In one embodiment, the forward primer hybridises to one or more of theCRISPR1 spacers labelled C, D, E, F, G, H, or I (see FIG. 3). Thereverse primer hybridises to one or more of the CRISPR1 spacers labelledM, N, O, P, Q, or R (see FIG. 3). Suitably, primers do not hybridise tothe spacer labelled as S. Typically, the amplified fragment will beabout 200 bp shorter with DSMZ18344 as compared to other strainsdescribed herein—such as CNCM I-2425.

In a further aspect, there is provided a method for identifying aStreptococcus thermophilus strain comprising the use of a forwardoligonucleotide primer which hybridises to SEQ ID No. 1 and a reverseoligonucleotide primer which hybridises to the SEQ ID No. 18.

In another aspect, there is provided a method for identifying aStreptococcus thermophilus strain comprising the use of a forwardoligonucleotide primer which hybridises to SEQ ID No. 1 and a reverseoligonucleotide primer which hybridises to any of SEQ ID No. 2, SEQ IDNo. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, SEQ ID No. 7, SEQ IDNo. 8, SEQ ID No. 9, SEQ ID No. 10, SEQ ID No. 11, SEQ ID No. 12, SEQ.ID No. 13, SEQ ID No. 14, SEQ ID No. 15, SEQ ID No. 16 and/or SEQ ID No.17.

In another aspect, there is provided a method for identifying aStreptococcus thermophilus strain comprising the use of a forwardoligonucleotide primer which hybridises to any of SEQ ID No. 2, SEQ IDNo. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, SEQ ID No. 7, SEQ IDNo. 8 and a reverse oligonucleotide primer why hybridises to any of SEQID No. 9, SEQ ID No. 10, SEQ ID No. 11, SEQ ID No. 12, SEQ ID No. 13,SEQ ID No. 14, SEQ ID No. 15, SEQ ID No. 16 and/or SEQ ID No. 17.

In another aspect, there is provided a method for identifying aStreptococcus thermophilus strain comprising the use of a forwardoligonucleotide primer which hybridises to any of SEQ ID No. 2, SEQ IDNo. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, SEQ ID No. 7 and/or SEQID No. 8 and reverse oligonucleotide primer which hybridises to SEQ IDNo. 18.

In another aspect, there is provided a method for identifying aStreptococcus thermophilus strain comprising the use of a forwardoligonucleotide primer which hybridises to any of SEQ ID No. 9, SEQ IDNo. 10, SEQ ID No. 11, SEQ ID No. 12, SEQ ID No. 13, SEQ ID No. 14, SEQID No. 15, SEQ ID No. 16 and/or SEQ ID No. 17 and a reverseoligonucleotide primer why hybridises to any SEQ ID No. 18. Preferably,forward and/or reverse oligonucleotide primers that hybridise to SEQ IDNo. 15 and SEQ ID No. 16 are not used.

The forward oligonucleotide primer may even hybridise to a sequence thatis upstream of SEQ ID No. 2.

The reverse primer may even hybridise to a sequence that is downstreamof SEQ ID No. 18.

Following amplification/detection, the amplified sequence may beidentified using various methods that are known in the art.

By way of example, the amplified sequence may be identified bydetermining the amplification product restriction pattern. Accordingly,once the DNA has been amplified, it may be digested (e.g. cut) with oneor more restriction enzymes.

As used herein, the term “restriction enzymes” refers to enzymes (e.g.bacterial enzymes), each of which cut double-stranded DNA at or near aspecific nucleotide sequence. Restriction enzymes are well known in theart and may be readily obtained, for example, from variety of commercialsources (for example, New England Biolabs, Inc., Beverly, Mass.).Similarly, methods for using restriction enzymes are also generally wellknown and routine in the art. Restriction enzymes that produce between10 and 24 fragments of DNA when cutting the CRISPR locus or a portionthereof may be used. Fragments of DNA obtained using restriction enzymesmay be detected, for example, as bands by gel electrophoresis.Restriction enzymes may be used to create Restriction Fragment LengthPolymorphisms (RFLPs).

RFLPs are generated by cutting (“restricting”) a DNA molecule with arestriction endonuclease. Many hundreds of such enzymes have beenisolated, as naturally made by bacteria. In essence, bacteria use suchenzymes as a defensive system, to recognise and then cleave (restrict)any foreign DNA molecules that might enter the bacterial cell (e.g., aviral infection). Each of the many hundreds of different restrictionenzymes has been found to cut (i.e., “cleave” or “restrict”) DNA at adifferent sequence of the 4 basic nucleotides (A, T, G, C) that make upall DNA molecules, e.g., one enzyme might specifically and onlyrecognise the sequence A-A-T-G-A-C, while another might specifically andonly recognise the sequence G-T-A-C-T-A, etc. Depending on the uniqueenzyme involved, such recognition sequences may vary in length, from asfew as 4 nucleotides to as many as 21 nucleotides. The larger therecognition sequence, the fewer restriction fragments will result, asthe larger the recognition site, the lower the probability that it willrepeatedly be found throughout the DNA.

By way of further example, the amplified sequence may be identified bydetermining or also determining the difference in size of theamplification product, as described above.

Separation may be achieved by any method suitable for separating DNA,including, but not limited to, gel electrophoresis, high performanceliquid chromatography (HPLC), mass spectroscopy, and use of amicrofluidic device. In one embodiment, the amplification products orDNA fragments are separated by agarose gel electrophoresis. Gelelectrophoresis separates different sized charged molecules by theirrate of movement through a stationary gel under the influence of anelectric current. These separated amplification products or DNAfragments can easily be visualised, for example, by staining withethidium bromide and by viewing the gel under UV illumination. Thebanding pattern reflects the sizes of the restriction digested DNA orthe amplification products.

By way of further example, the amplified sequence may be identified bysequencing the amplification products.

The sequence of the amplified products may be obtained by any methodknown in the art, including automatic and manual sequencing methods.See, for example, Sambrook et al. (1989) Molecular Cloning: A LaboratoryManual (2d ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y.;Roe et al. (1996) DNA Isolation and Sequencing (Essential TechniquesSeries, John Wiley & Sons).

Preferably, the Streptococcus thermophilus that is identified inaccordance with the methods of the present invention has substantiallythe same characteristics as the Streptococcus thermophilus straindeposited at DSMZ (Deutsche Sammlung von Mikroorganismen undZellkulturen GmbH, Mascheroder Weg 1 b, D-38124 Braunschweig) underdeposit number 18344 on 14 Jun. 2006. In the context of the presentinvention, the phrase “substantially the same characteristics” meansthat the Streptococcus thermophilus strain has one or more (preferablyall) of the characteristics of the Streptococcus thermophilus straindeposited at DSMZ (Deutsche Sammlung von Mikroorganismen undZellkulturen GmbH, Mascheroder Weg 1 b, D-38124 Braunschweig) underdeposit number 18344 on 14 Jun. 2006.

Suitably, the Streptococcus thermophilus that is identified is a fastacidifying lactic acid bacterium; and/or the Streptococcus thermophilusthat is identified generates a viscosity in fermented milk greater thanabout 62 Pa·s, preferably about 68 Pa·s; and/or the Streptococcusthermophilus that is identified is phage resistant; and/or theStreptococcus thermophilus that is identified belongs to the geneticcluster CL0189; and/or the Streptococcus thermophilus that is identifiedcomprises the sequence set forth in SEQ ID No. 20; and/or theStreptococcus thermophilus that is identified comprises the sequence setforth in SEQ ID No. 19 or a variant, fragment, homologue or derivativethereof.

CRISPR Orientation

For the avoidance of doubt, in the context of the present invention theCRISPR locus is orientated as follows.

The CRISPR leader is a conserved DNA segment of defined size. Forexample, the leader sequence of S. thermophilus LMG18311 (AccessionCP000024) CRISPR1 is the DNA segment starting immediately after the stopcodon of gene stu0660, and ending just before the first repeat. TheCRISPR leader is located at the 5′ end of the CRISPR locus. The CRISPRleader is located immediately upstream of the first CRISPR repeat of theCRISPR locus.

The CRISPR trailer is a conserved DNA segment of defined size. Forexample, the trailer sequence of S. thermophilus LMG18311 (AccessionCP000024) CRISPR1 is the DNA segment starting immediately after theterminal repeat, and ending just before the stop codon of gene stu0661(located on the opposite DNA strand). The CRISPR trailer is located atthe 3′ end of the CRISPR locus. The CRISPR trailer is locatedimmediately downstream of the terminal repeat.

By way of example, the CRISPR leader and CRISPR trailer sequences in theCRISPR1 locus of Streptococcus thermophilus strain CNRZ 1066 are:

CRISPIR leader5′-CAAGGACAGTTATTGATTTTATAATCACTATGTGGGTATAAAAACGTCAAAATTTCATTTGAG-3′CRISPR trailer 5′-TTGATTCAACATAAAAAGCCAGTTCAATTGAACTTGGCTTT-3′

The CRISPR leader corresponds to positions 625038 to 625100, and theCRISPR trailer corresponds to positions 627845 to 627885 in the fullgenome (CP000024) of Streptococcus thermophilus.

For the avoidance of doubt “upstream” means in the 5′ direction and“downstream” means in the 3′ direction.

EPS

Lactic bacteria are known to be capable of producing two classes ofpolysaccharides in their culture medium, namely homopolysaccharides suchas dextrans or levans which consist of the repeated assembly of a singlesugar, and heteropolysaccharides commonly called exopolysaccharides orEPSs (EPS is short for the term “exopolysaccharide”) consisting of theassembly of several different sugars forming a repeating unit (CerningJ., Bacteries lactiques, [Lactic bacteria], Vol I, by de Roissart H andLuquet F. M., Lorica, 309-329, 1994).

A lactic bacterium producing an EPS can impart a ropy character and/or asmooth and creamy texture to an acidified milk (Cerning et al., FEMSMicrobiol., 87, 113-130, 1990). EPSs can also display biologicalactivities which are especially advantageous for human or animal health,such as antitumour or probiotic activities, for example (Oda M. et al.,Agric. Biol. Chem., 47, 1623-1625, 1983; EP94870139.6).

Distinct EPS gene clusters have been characterised in S. thermophilus.The distribution of regulatory and structural genes within each of theseclusters shows a modular organisation that is conserved in otherStreptococcus spp. Although the function of most EPS-related genes(currently designated eps or cps) and gene products are only inferredfrom sequence or structural homologies, the 5′ region of each clusterappears to encode proteins involved in regulation of EPS synthesis,chain length determination, and membrane translocation. These openreading frames are followed by genes encoding the glycosyl-1-phosphatetransferase and glycosyltransferases required for assembly of the basicrepeating unit, and enzymes involved in repeat unit polymerization.Finally, the 3′ end of these clusters typically contain genes foradditional proteins involved in membrane translocation of the polymersubunits, and enzymes needed for the production of sugar nucleotideprecursors (e.g., N-acetyl-D-galactosamine; that are unique to the EPS(i.e., not found in other cell polymers).

The first four genes in the 5′ region of S. thermophilus eps clusters,epsA-D, are highly conserved among this and other EPS⁺ Streptococcus sppappear to contribute regulation (epsA and epsB), polymerization (epsC),and membrane translocation (epsD) functions to EPS synthesis. epsEencodes a glycosyl-1-phosphate transferase that catalyzes the first stepin assembly of the EPS basic repeating unit: addition ofhexose-1-phosphate to the lipid-phosphate carrier. Genes downstream ofepsE appear to encode glycosyltransferases, export/polymerizationfunctions, sugar biosynthesis, and a few enzymes whose function isunknown. Genes encoding a variety of glycosyltransferases have beenidentified in S. thermophilus and other lactic acid bacteria.

The lactic acid bacterium according to the present invention comprisesan EPS gene cluster comprising the sequence set forth in SEQ ID No. 20or a variant, fragment, homologue or derivative thereof.

Surprisingly, the lactic acid bacterium described herein has high epssequence similarity with S. thermophilus CNCM I-2425 from the start ofthe eps gene cluster sequence up to about position 3900 (ie. in epsEgene) and high eps sequence similarity with S. thermophilus CNCM I-2423from about position 3900 to the end of the sequence.

Hybridisation

The present invention also encompasses sequences that are complementaryto the sequences of the present invention or sequences that are capableof hybridising either to the sequences of the present invention or tosequences that are complementary thereto.

The term “hybridisation” as used herein shall include “the process bywhich a strand of nucleic acid joins with a complementary strand throughbase pairing” as well as the process of amplification as carried out inpolymerase chain reaction (PCR) technologies.

The present invention also encompasses the use of nucleotide sequencesthat are capable of hybridising to the sequences that are complementaryto the subject sequences discussed herein, or any derivative, fragmentor derivative thereof.

The present invention also encompasses sequences that are complementaryto sequences that are capable of hybridising to the nucleotide sequencesdiscussed herein.

Hybridisation conditions are based on the melting temperature (Tm) ofthe nucleotide binding complex, as taught in Berger and Kimmel (1987,Guide to Molecular Cloning Techniques, Methods in Enzymology, Vol. 152,Academic Press, San Diego Calif.), and confer a defined “stringency” asexplained below.

Maximum stringency typically occurs at about Tm-5° C. (5° C. below theTm of the probe); high stringency at about 5° C. to 10° C. below Tm;intermediate stringency at about 10° C. to 20° C. below Tm; and lowstringency at about 20° C. to 25° C. below Tm. As will be understood bythose of skill in the art, a maximum stringency hybridisation can beused to identify or detect identical nucleotide sequences while anintermediate (or low) stringency hybridisation can be used to identifyor detect similar or related polynucleotide sequences.

Preferably, the present invention encompasses sequences that arecomplementary to sequences that are capable of hybridising under highstringency conditions or intermediate stringency conditions tonucleotide sequences encoding polypeptides having the specificproperties as defined herein.

More preferably, the present invention encompasses sequences that arecomplementary to sequences that are capable of hybridising under highstringent conditions (e.g. 65° C. and 0.1×SSC {1×SSC=0.15 M NaCl, 0.015M Na-citrate pH 7.0}) to nucleotide sequences encoding polypeptideshaving the specific properties as defined herein.

The present invention also relates to nucleotide sequences that canhybridise to the nucleotide sequences discussed herein (includingcomplementary sequences of those discussed herein).

The present invention also relates to nucleotide sequences that arecomplementary to sequences that can hybridise to the nucleotidesequences discussed herein (including complementary sequences of thosediscussed herein).

Also included within the scope of the present invention arepolynucleotide sequences that are capable of hybridising to thenucleotide sequences discussed herein under conditions of intermediateto maximal stringency.

In a preferred aspect, the present invention covers nucleotide sequencesthat can hybridise to the nucleotide sequences discussed herein, or thecomplement thereof, under stringent conditions (e.g. 50° C. and0.2×SSC).

In a more preferred aspect, the present invention covers nucleotidesequences that can hybridise to the nucleotide sequences discussedherein, or the complement thereof, under high stringent conditions (e.g.65° C. and 0.1×SSC).

Substantially

Suitably, the oligonucleotide primers described herein substantiallyanneal or substantially hybridise to its respective nucleic acid. Thismeans that an oligonucleotide—such as a primer—should be sufficientlycomplementary to hybridise or anneal to its respective nucleic acid.

The oligonucleotide sequence need not reflect the exact sequence of itsrespective nucleic acid, and can, in fact, be “degenerate”.Non-complementary bases or other sequences may be interspersed into theoligonucleotide or the nucleic acid, provided that the oligonucleotidesequence has sufficient complementarity with the sequence to permithybridisation. Thus, by way of example, the primers used for PCRamplification may be selected to be “substantially” complementary to thespecific sequence to be amplified.

Starter Cultures

Starter cultures are used extensively in the food industry in themanufacture of products (e.g. fermented products) including milkproducts—such as yoghurt and cheese.

Starter cultures used in the manufacture of many fermented milk, cheeseand butter products include cultures of bacteria, generally classifiedas lactic acid bacteria. Such bacterial starter cultures impart specificfeatures to various dairy products by performing a number of functions.

Commercial non-concentrated cultures of bacteria are referred to inindustry as ‘mother cultures’, and are propagated at the productionsite, for example a dairy, before being added to an edible startingmaterial, such as milk, for fermentation. The starter culture propagatedat the production site for inoculation into an edible starting materialis referred to as the ‘bulk starter’.

The bacterial starter culture may consist of the lactic acid bacteriumdescribed herein, ie., a pure culture. In this case, substantially all,or at least a significant portion of the bacterial starter culture wouldgenerally comprise the same bacterium.

In the alternative, the starter culture may comprise several bacterialstrains, ie. it may be a defined mixed culture.

For example, the starter culture may be suitable for use in the dairyindustry. When used in the dairy industry the starter culture mayadditionally comprise a lactic acid bacteria species, a Bifidobacteriumspecies, a Brevibacterium species, and/or a Propionibacterium species.

Cultures of lactic acid bacteria are commonly used in the manufacture offermented milk products—such as buttermilk, yoghurt or sour cream, andin the manufacture of butter and cheese, for example Brie or Harvati.

Suitable lactic acid bacteria include commonly used strains of aLactococcus species, a Streptococcus species, a Lactobacillus speciesincluding the Lactobacillus acidophilus, Enterococcus species,Pediococcus species, a Leuconostoc species and Oenococcus species orcombinations thereof.

Lactococcus species include the widely used Lactococcus lactis,including Lactococcus lactis subsp. Lactis, Lactococcus lactis subsp.lactis biovar diacetylactis and Lactococcus lactis subsp. cremoris.

Other lactic acid bacteria species include Leuconostoc sp.,Streptococcus thermophilus, Lactobacillus delbrueckii subsp. bulgaricusand Lactobacillus helveticus. Mesophilic cultures of lactic acidbacteria commonly used in the manufacture of fermented milk productssuch as buttermilk, yoghurt or sour cream, and in the manufacture ofbutter and cheese, for example Brie or Harvati. In addition, probioticstrains such as Bifidobacterium lactis, Lactobacillus acidophilus,Lactobacillus casei may be added during said manufacturing to enhanceflavour or to promote health.

Cultures of lactic acid bacteria commonly used in the manufacture ofcheddar and Monterey Jack cheeses include Streptococcus thermophilus,Lactococcus lactis subsp. lactis and Lactococcus lactis subsp. cremorisor combinations thereof.

Thermophilic cultures of lactic acid bacteria commonly used in themanufacture of Italian cheeses such as Pasta filata or parmesan, includeStreptococcus thermophilus and Lactobacillus delbrueckii subspbulgaricus. Other Lactobacillus species—such as Lactobacillushelveticus—may be added during manufacturing to obtain a desiredflavour.

The selection of organisms for the starter culture of the invention willdepend on the particular type of products to be prepared and treated.Thus, for example, for cheese and butter manufacturing, mesophilliccultures of Lactococcus species, Leuconostoc species and Lactobacillusspecies are widely used, whereas for yoghurt and other fermented milkproducts, thermophillic strains of Streptococcus species and ofLactobacillus species are typically used.

The starter culture may even be a dried starter culture.

The starter culture may be a concentrated starter culture. The starterculture may be a concentrated starter culture used in directinoculation. The starter culture may be a frozen starter culture.

Preparing Starter Cultures

Starter cultures may be prepared by techniques well known in the artsuch as those disclosed in U.S. Pat. No. 4,621,058. By way of example,starter cultures may be prepared by the introduction of an inoculum, forexample a bacterium, to a growth medium to produce an inoculated mediumand ripening the inoculated medium to produce a starter culture.

Preparing Dried Starter Cultures

Dried starter cultures may be prepared by techniques well known in theart, such as those discussed in U.S. Pat. No. 4,423,079 and U.S. Pat.No. 4,140,800.

Dried starter cultures for use in the present invention may be in theform of solid preparations. Examples of solid preparations include, butare not limited to tablets, pellets, capsules, dusts, granules andpowders which may be wettable, spray-dried, freeze-dried or lyophilised.

The dried starter cultures for use in the present invention may be ineither a deep frozen pellet form or freeze-dried powder form. Driedstarter cultures in a deep frozen pellet or freeze-dried powder form maybe prepared according to the methods known in the art.

The starter cultures for use in the present invention may be in the formof concentrates which comprise a substantially high concentration of oneor more bacteria. Preferably the concentrates may be diluted with wateror resuspended in water or other suitable diluents, for example, anappropriate growth medium or mineral or vegetable oils, for use in thepresent invention. The dried starter cultures of the present inventionin the form of concentrates may be prepared according to the methodsknown in the art, for example by centrifugation, filtration or acombination of such techniques.

Product

Any product, which is prepared from, contains or comprises a lactic acidbacterium is contemplated in accordance with the present invention.

Suitable products include, but are not limited to a food, a foodstuff, afood additive, a food supplement, a feed, a nutritional supplement, aprobiotic supplement, a cosmetic product or a pharmaceutical product.

These include, but are not limited to, fruits, legumes, fodder crops andvegetables including derived products, grain and grain-derived products,dairy foods and dairy food-derived products, meat, poultry and seafood.

The term “food” is used in a broad sense and includes feeds, foodstuffs,food ingredients, food supplements, and functional foods. Here, the term“food” is used in a broad sense—and covers food for humans as well asfood for animals (i.e. a feed). In a preferred aspect, the food is forhuman consumption.

As used herein the term “food ingredient” includes a formulation, whichis or can be added to foods and includes formulations which can be usedat low levels in a wide variety of products that require, for example,acidifying or emulsifying.

As used herein, the term “functional food” means a food which is capableof providing not only a nutritional effect and/or a taste satisfaction,but is also capable of delivering a further beneficial effect toconsumer. Although there is no legal definition of a functional food,most of the parties with an interest in this area agree that there arefoods marketed as having specific health effects.

The bacteria described herein may be—or may be added to—a foodingredient, a food supplement, or a functional food.

The food may be in the form of a solution or as a solid—depending on theuse and/or the mode of application and/or the mode of administration.

The bacteria described here can be used in the preparation of foodproducts such as one or more of: confectionery products, dairy products,meat products, poultry products, fish products and bakery products.

By way of example, the bacteria can be used as ingredients to softdrinks, a fruit juice or a beverage comprising whey protein, healthteas, cocoa drinks, milk drinks and lactic acid bacteria drinks,yoghurt, drinking yoghurt and wine.

The present invention also provides in a further aspect a method ofpreparing a food, food additive, feed, nutritional supplement orprobiotic supplement, the method comprising admixing the lactic acidbacterium according to the present invention with a food, food additive,feed, nutritional supplement, probiotic supplement and/or food or feedingredient (such as a starting material for a food).

Preferably a food as described herein is a dairy product. Morepreferably, a dairy product as described herein is one or more of thefollowing: a yoghurt, a cheese (such as an acid curd cheese, a hardcheese, a semi-hard cheese, a cottage cheese), a buttermilk, quark, asour cream, kefir, a fermented whey-based beverage, a koumiss, a milkbeverage, a yoghurt drink, a fermented milk, a matured cream, a cheese,a fromage frais, a milk, a dairy product retentate, a process cheese, acream dessert, or infant milk.

Preferably, a food as described herein is a fermented food product. Morepreferably, a food as described herein is a fermented dairy product—suchas a milk beverage, a yoghurt drink, a fermented milk, a matured cream,a cheese, a fromage frais, a dairy product retentate, a process cheese,a cream dessert, or infant milk.

Preferably the dairy product according to the invention comprises milkof animal and/or plant origin.

Milk is understood to mean that of animal origin, such as cow, goat,sheep, buffalo, zebra, horse, donkey, or camel, and the like. The milkmay be in the native state, a reconstituted milk, a skimmed milk or amilk supplemented with compounds necessary for the growth of thebacteria or for the subsequent processing of fermented milk, such asfat, proteins of a yeast extract, peptone and/or a surfactant, forexample. The term milk also applies to what is commonly called vegetablemilk, that is to say extracts of plant material which have been treatedor otherwise, such as leguminous plants (soya bean, chick pea, lentiland the like) or oilseeds (colza, soya bean, sesame, cotton and thelike), which extract contains proteins in solution or in colloidalsuspension, which are coagulable by chemical action, by acidfermentation and/or by heat. Finally, the word milk also denotesmixtures of animal milks and of vegetable milks.

In one embodiment, the term “milk” means commercial UHT milksupplemented with 3% (w/w) of semi-skimmed milk powder pasteurized byheating during 10 min+/−1 min. at 90° C.+/−0.2° C.

In a further aspect there is provided a method for preparing a fermentedmilk product wherein said process comprises fermenting a milk substratein the presence of at least the lactic acid bacterium, the culture orthe starter culture described herein. Preferably, the milk substrate ismilk. Preferably, the milk substrate comprises solid items. Preferably,the solid items comprise or consist of fruits, chocolate products, orcereals.

Sequence

For some embodiments of the present invention, it is preferred that thesequence is a naturally occurring nucleic acid sequence.

The nucleic acid sequence may be DNA or RNA of genomic, synthetic orrecombinant origin e.g. cDNA. The nucleotide sequence may bedouble-stranded or single-stranded whether representing the sense orantisense strand or combinations thereof. Recombinant nucleic acidsequences may be prepared by use of recombinant DNA techniques, asdescribed herein.

The nucleic acid sequence and the nucleic acids encompassed by thepresent invention may be isolated or substantially purified. By“isolated” or “substantially purified” is intended that the nucleic acidmolecules, or biologically active fragments or variants, homologues orderivatives thereof are substantially or essentially free fromcomponents normally found in association with the nucleic acid in itsnatural state. Such components include other cellular material, culturemedia from recombinant production, and various chemicals used inchemically synthesising the nucleic acids.

An “isolated” nucleic acid sequence or nucleic acid is typically free ofnucleic acid sequences that flank the nucleic acid of interest in thegenomic DNA of the organism from which the nucleic acid was derived(such as coding sequences present at the 5′ or 3′ ends). However, themolecule may include some additional bases or moieties that do notdeleteriously affect the basic characteristics of the composition.

In one aspect, there is provided the nucleotide sequence set forth inSEQ ID No. 19 or fragment, variant, homologue or derivative thereof.

In a further aspect, there is provided the sequence set forth in SEQ IDNo. 19 or a homologue thereof with at least 75% identity thereto.

Suitably, the sequence set forth in SEQ ID No. 19 or a homologue thereofhas at least 75% identity thereto, when the full length CRISPR loci arealigned.

Variants/Homologues/Derivatives/Fragments

The present invention encompasses the use of variants, homologues,derivatives and fragments of nucleic acid sequences.

The term “variant” is used to mean a naturally occurring nucleotidesequence which differs from a wild-type sequence.

The term “fragment” indicates that a nucleotide sequence comprises afraction of a wild-type sequence. It may comprise one or more largecontiguous sections of sequence or a plurality of small sections.Preferably the sequence comprises at least 50%, more preferably at least65%, more preferably at least 80%, more preferably at least 85%, morepreferably at least 90%, more preferably at least 95%, more preferablyat least 96%, more preferably at least 97%, more preferably at least98%, most preferably at least 99% of the wild-type sequence.

Preferably, the fragment retains 50%, more preferably 60%, morepreferably 70%, more preferably 80%, more preferably 85%, morepreferably 90%, more preferably 95%, more preferably 96%, morepreferably 97%, more preferably 98%, or most preferably 99% activity ofthe wild-type nucleotide sequence.

The fragment may be a functional fragment.

By a “functional fragment” of a molecule is understood a fragmentretaining or possessing substantially the same biological activity asthe intact molecule. In all instances, a functional fragment of amolecule retains at least 10% and at least about 25%, 50%, 75%, 80%,85%, 90%, 95%, 96%, 97%, 98% or 99% of the biological activity of theintact molecule.

The term “homologue” means an entity having a certain homology with thesubject nucleotide sequences. Here, the term “homology” can be equatedwith “identity”.

In the present context, a homologous sequence is taken to include anucleotide sequence, which may be at least 60, 70, 75, 85 or 90%identical, preferably at least 95%, 96%, 97%, 98% or 99% identical tothe subject sequence. Although homology can also be considered in termsof similarity, in the context of the present invention it is preferredto express homology in terms of sequence identity.

Homology comparisons may be conducted by eye, or more usually, with theaid of readily available sequence comparison programs. Thesecommercially available computer programs can calculate % homologybetween two or more sequences.

% homology may be calculated over contiguous sequences. This is calledan “ungapped” alignment. Typically, such ungapped alignments areperformed only over a relatively short number of residues.

Most sequence comparison methods are designed to produce optimalalignments that take into consideration possible insertions anddeletions without penalising unduly the overall homology score. This isachieved by inserting “gaps” in the sequence alignment to try tomaximise local homology.

However, these more complex methods assign “gap penalties” to each gapthat occurs in the alignment. “Affine gap costs” are typically used thatcharge a relatively high cost for the existence of a gap and a smallerpenalty for each subsequent residue in the gap. This is the mostcommonly used gap scoring system. High gap penalties will of courseproduce optimised alignments with fewer gaps. Most alignment programsallow the gap penalties to be modified. However, it is preferred to usethe default values when using such software for sequence comparisons.For example, when using the GCG Wisconsin Bestfit package the defaultgap penalty for amino acid sequences is −12 for a gap and −4 for eachextension.

Calculation of maximum % homology therefore firstly requires theproduction of an optimal alignment, taking into consideration gappenalties. A suitable computer program for carrying out such analignment is the GCG Wisconsin Bestfit package (University of Wisconsin,U.S.A.; Devereux et al., 1984, Nucleic Acids Research 12:387). Examplesof other software than can perform sequence comparisons include, but arenot limited to, the BLAST package (see Ausubel et al., 1999 ibid—Chapter18), FASTA (Atschul et al., 1990, J. Mol. Biol., 403-410), the GENEWORKSsuite of comparison tools and CLUSTAL. Both BLAST and FASTA areavailable for offline and online searching (see Ausubel et al., 1999ibid, pages 7-58 to 7-60). However, for some applications, it ispreferred to use the GCG Bestfit program. A new tool, called BLAST 2Sequences is also available for comparing protein and nucleotidesequence (see FEMS Microbiol Lett 1999 174(2): 247-50; FEMS MicrobiolLett 1999 177(1): 187-8).

Although the final % homology can be measured in terms of identity, thealignment process itself is typically not based on an all-or -nothingpair comparison. Instead, a scaled similarity score matrix is generallyused that assigns scores to each pairwise comparison based on chemicalsimilarity or evolutionary distance. An example of such a matrixcommonly used is the BLOSUM62 matrix—the default matrix for the BLASTsuite of programs. GCG Wisconsin programs generally use either thepublic default values or a custom symbol comparison table if supplied(see user manual for further details). For some applications, it ispreferred to use the public default values for the GCG package, or inthe case of other software, the default matrix—such as BLOSUM62.

Once the software has produced an optimal alignment, it is possible tocalculate % homology, preferably % sequence identity. The softwaretypically does this as part of the sequence comparison and generates anumerical result.

Should Gap Penalties be used when determining sequence identity, thenpreferably the following parameters are used:

FOR BLAST GAP OPEN 0 GAP EXTENSION 0

FOR CLUSTAL DNA PROTEIN WORD SIZE 2 1 K triple GAP PENALTY 10 10 GAPEXTENSION 0.1 0.1

The nucleotide sequences may include within them synthetic or modifiednucleotides. A number of different types of modification tooligonucleotides are known in the art. These include methylphosphonateand phosphorothioate backbones and/or the addition of acridine orpolylysine chains at the 3′ and/or 5′ ends of the molecule. For thepurposes of the present invention, it is to be understood that thenucleotide sequences may be modified by any method available in the art.Such modifications may be carried out to enhance the in vivo activity orlife span of nucleotide sequences useful in the present invention.

Vector

The nucleotide sequence(s) described herein may be present in a vector.The nucleotide sequence may be operably linked to regulatory sequencessuch that the regulatory sequences are capable of providing for theexpression of the nucleotide sequence by a suitable host organism ie.the vector may be an expression vector.

The term “expression vector” means a construct capable of in vivo or invitro expression.

Preferably, the expression vector is incorporated in the genome of theorganism. The term “incorporated” preferably covers stable incorporationinto the genome.

The vectors may be transformed into a suitable host cell as describedbelow to provide for expression of a polypeptide having the specificproperties as defined herein.

The choice of vector, e.g. plasmid, cosmid, virus or phage vector, willoften depend on the host cell into which it is to be introduced.

The vectors may contain one or more selectable marker genes—such as agene which confers antibiotic resistance e.g. ampicillin, kanamycin,chloramphenicol or tetracyclin resistance. Alternatively, the selectionmay be accomplished by co-transformation (as described in WO91/17243).

The vector may further comprise a nucleotide sequence enabling thevector to replicate in the host cell in question. Examples of suchsequences are the origins of replication of plasmids pUC19, pACYC177,pUB110, pE194, pAMB1 and pIJ702.

Constructs

The term “construct”—which is synonymous with terms such as “conjugate”,“cassette” and “hybrid”—includes a nucleotide sequence directly orindirectly attached to a promoter. An example of an indirect attachmentis the provision of a suitable spacer group such as an intron sequence,such as the Sh1-intron or the ADH intron, intermediate the promoter andthe nucleotide sequence of the present invention. The same is true forthe term “fused” in relation to the present invention, which includesdirect or indirect attachment. In some cases, the terms do not cover thenatural combination of the nucleotide sequence coding for the proteinordinarily associated with the wild type gene promoter and when they areboth in their natural environment.

The construct may even contain or express a marker, which allows for theselection of the genetic construct.

For some applications, preferably the construct comprises at least anucleotide sequence operably linked to a promoter.

Host Cells

The term “host cell” includes any cell that comprises a nucleotidesequence, a construct or a vector.

The cells will be chosen to be compatible with the said vector and mayfor example be prokaryotic (for example bacterial), fungal, yeast orplant cells. Preferably, the host cells are not human cells.

Examples of suitable bacterial host organisms are gram negativebacterium or gram positive bacteria.

General Recombinant DNA Methodology Techniques

The present invention employs, unless otherwise indicated, conventionaltechniques of biochemistry, molecular biology, microbiology andrecombinant DNA, which are within the capabilities of a person ofordinary skill in the art. Such techniques are explained in theliterature. See, for example, J. Sambrook, E. F. Fritsch, and T.Maniatis, 1989, Molecular Cloning: A Laboratory Manual, Second Edition,Books 1-3, Cold Spring Harbor Laboratory Press; Ausubel, F. M. et al.(1995 and periodic supplements; Current Protocols in Molecular Biology,ch. 9, 13, and 16, John Wiley & Sons, New York, N.Y.); B. Roe, J.Crabtree, and A. Kahn, 1996, DNA Isolation and Sequencing: EssentialTechniques, John Wiley & Sons; M. J. Gait (Editor), 1984,Oligonucleotide Synthesis: A Practical Approach, Irl Press; and, D. M.J. Lilley and J. E. Dahlberg, 1992, Methods of Enzymology: DNA StructurePart A: Synthesis and Physical Analysis of DNA Methods in Enzymology,Academic Press. Each of these general texts is herein incorporated byreference.

Further Aspects

In a further aspect, there is provided a lactic acid bacteriumcomprising the sequence set forth in SEQ ID No. 20 or a variant,fragment, homologue or derivative thereof, preferably, a homologuethereof with at least 99% identity thereto.

In a further aspect, there is provided a nucleotide sequence comprisingthe sequence set forth in SEQ ID No. 20 or a variant, fragment,homologue or derivative thereof, preferably, a homologue thereof with atleast 99% identity thereto.

In a further aspect, there is provided a method for identifying a lacticacid bacterium comprising the step of screening a bacterium for thesequence set forth in SEQ ID No. 20 or a variant, fragment, homologue orderivative thereof, preferably, a homologue thereof with at least 99%identity thereto.

In a further aspect, there is provided a micro-organism a Streptococcusthermophilus strain deposited under the Budapest Treaty by DaniscoDeutschland Niebüll GmbH, Buch-Johannsen Strasse. 1, Niebüll -D-25899,Germany at DSMZ (Deutsche The spacers of the CRISPR 1 locus of S.thermophilus DSMZ-18344 have been sequenced and compared to that of S.thermophilus CNCM I-2425, S. thermophilus CNCM I-2423 and other spacersequences. The only similarities were found with S. thermophilus CNRZ385 (Genbank accession number DQ072992) and CNCM I-2425 (and relatedstrains). Interestingly, the spacers within this CRISPR locus have adifferent organisation (5 missing spacers) and 1 additional spacer wereidentified.

The lysotype of S. thermophilus DSMZ-18344 and the differences observedbetween the lysotype of S. thermophilus DSMZ-18344 and strains of theCL0189 genotype are shown in Table 2.

Example 5 S. thermophilus DSMZ-18344 is Phage Resistant

Over the last 2 decades a library of more than one thousand phagesvirulent for industrial S. thermophilus strains have been collated. Thiscollection of phages was intensively studied and their host spectrum wasestablished. This allowed the identification of a set of 60 phagesrepresentative of all the host spectrums identified within thecollection of phages.

Each of these representative phages was tested on strains DSMZ18344,CNCM I-2423 and CNCM I-2425, as described herein.

CNCM I-2423 was found to be sensitive to phage D4126 and D3215. StrainCNCMI-2425 was found to be sensitive to phage D4369. On the contrarystrain DSMZ-18344 was resistant to all the representative phages tested.

TABLE 1 Strain Viscosity Casson yield stress Thixotropy area name (Pa ·s) (Pa) (Pa/s) DSMZ-18344 68 6.48 627 CNCM I-2425 28 14.43 21780 CNCMI-2423 49 9.28 1035

Sammlung von Mikroorganismen und Zellkulturen GmbH, Mascheroder Weg 1 b,D-38124 Braunschweig) under deposit number 18344 on 14 Jun. 2006 or amutant or variant thereof having one of or more of the characteristicsof the deposited Streptococcus thermophilus strain.

The invention will now be further described by way of Examples, whichare meant to serve to assist one of ordinary skill in the art incarrying out the invention and are not intended in any way to limit thescope of the invention.

EXAMPLES Example 1 Streptococcus thermophilus DSMZ-18344 is a FastAcidifier of Milk

The speed of acidification of milk during the fermentation process is−0.0153 upH/min, compared to 0.0129 upH/min, 0.0167 upH/min and 0.0209upH/min for Streptococcus thermophilus CNCM I-2423, Streptococcusthermophilus CNCM I-2980 and Streptococcus thermophilus CNCM I-2425,respectively.

Example 2 Streptococcus thermophilus DSMZ-18344 Generates Fermented Milkwith a Superior Viscosity

Fresh fermented milks are produced at lab scale. The milk base iscomposed of commercial UHT milk supplemented with 3% (w/w) semi-skimmedmilk powder. After mixing, the milk base is heated during 10 min+/−1 minat 90° C.+/−0.2° C. The base is then cooled down at 43° C.+/−1° C. in awater bath regulated at 43° C.+/−1° C. and the milk is dispatched into125 ml glass beakers.

The milk is inoculated with the bacterium at a ratio of 1E6-1E7 cfu/ml.The fermentation is carried out at 43° C.+/−1° C. with out stirring andit is stopped when the pH reaches 4.6+/−0.05. At this moment, the freshfermented milk is quickly cooled down at 6° C.+/1° C. in less than 1hour. Finally, the products are stored at this temperature during 28days.

Following this production of fermented milk either viscosimetry ismeasured using a Brookfield viscosimeter.

The viscosity in fermented milk is 68 Pa·s after 14 days of storage at6° C.

Usually a strain identified as highly texturizing generates fermentedmilk with a viscosity superior to 45 Pa·s, a Casson yield stressinferior to 12.0 Pa and a thixotropy area inferior to 1000 Pa/s.

A comparison of the rheological properties of three texturizing S.thermophilus strains are shown in Table 1.

Example 3 Molecular Analysis of Streptococcus thermophilus DSMZ-18344

The EPSAD PCR-RFLP method is a molecular method to establish geneticlineage between strains of S. thermophilus.

Streptococcus thermophilus genomic DNA is purified using the DNeasyTissue Kit (Qiagen). Purified DNA is then amplified by PCR with thefollowing parameters:

Composition of the PCR reaction mix (50 μL):

-   -   buffer for DNA polymerase ×1    -   MgCl₂ 2 mM    -   dNTP 200 μM each    -   genomic DNA 100 to 500 ng    -   primer EPSA632 (5′-AAATgAATTCAgAgCAAgCACTTg-3′) 200 nM    -   primer EPSD1064 (5′-gTCATgTCAACTTTATTAAggACg-3′) 200 nM    -   DNA polymerase 1.25 unit    -   H₂O qsp 50 μL

Amplification Parameters:

-   -   predenaturation at 94° C. during 1 min    -   cycles with denaturation at 94° C. during 30 s, hybridization at        56° C. during 30 s, elongation at 72° C. during 3 min    -   post-elongation at 72° C. during 6 min.

After amplification, the PCR product is checked by 1.5% agarose gelelectrophoresis. The size of the amplification product is about 2.5 kb.

The PCR product is then digested by two restriction enzymes FokI et MnlIin the following conditions:

-   -   PCR product 15 to 30 μL    -   buffer 2 (New England Biolabs) ×1    -   BSA (New England Biolabs) ×1    -   FokI (New England Biolabs) 1 unit    -   MnlI (New England Biolabs) 1 unit    -   H2O qsp 50 μL

Incubation at 37° C. during 1 hour.

The digested product is analysed by 3% agarose gel electrophoresis.

Applied to S. thermophilus DSMZ-18344, it groups this strain within agenetic cluster known as CL0189. This was further confirmed by thesequencing of the proximal part of its eps operon (that is the targetedchromosomal region with the EPSAD method).

The EPSAD PCR-RFLP profile of S. thermophilus DSMZ-18344 is shown inFIG. 1.

Referring to this Figure, S. thermophilus DSMZ-18344 shows geneticlineage to S. thermophilus CNCM I-2425 profile which is therepresentative strain of the CL0189 genetic cluster.

The distal part of the eps operon was also sequenced and compared tothat available in the literature. Unexpectedly, this part of the S.thermophilus DSMZ-18344 eps operon is distinct to that of strain S.thermophilus CNCM I-2425. However, it is very similar to that of S.thermophilus CNCM I-2423 and other strains within the S. thermophilusCNCM I-2423 genetic cluster (namely CL0089 that also contains S.thermophilus CNCM I-2426 and S. thermophilus Sfi39 (Genbank entryAF373595).

Schematic organisation of the distal part of the eps operon andsimilarities between strains are shown in FIG. 2.

The sequence data on the distal part of the eps operon and the EPSADclustering data together suggest that the eps operon of S. thermophilusDSMZ-18344 is a chimeric operon made of the proximal part of the operoncoming from S. thermophilus CNCM 1-2425 (or related strains) and thedistal part of the operon coming from S. thermophilus CNCM I-2423 (orrelated strains).

This unusual feature may be useful to develop a method to specificallydetect S. thermophilus DSMZ-18344 (or related strains from other S.thermophilus) as described herein.

The strain S. thermophilus CNCM I-2423 is one of the fast acidifyingstrains that presents texturizing properties of interest in fermentedmilk whereas S. thermophilus CNCM I-2425 even if fast acidifying doesnot have these interesting texturing properties. In S. thermophilus, thedistal part of the eps operon contains genes that code for glycosyltransferases. These enzymes are known to be responsible of the structureof the polysaccharidic units composing the exopolysaccharide and thenature of this exopolysaccharide is at least partly believed to beresponsible of the texturizing properties of a strain. Therefore, thechimeric structure of the eps operon may explain its texturingcapabilities.

Example 4 CRISPR Spacers of S. thermophilus DSMZ-18344

The spacer sequences in the CRISPR locus are genetic features that arevery specific to a strain or to related strains.

TABLE 2 Sensitivity to Sensitivity to Sensitivity to Distal part of CNCMI-2425 CNCM I-2423 other Strain Genotype eps operon phages phages phagesTexturing DSMZ-18344 CL0189 CNCM I-2423 type No No No Yes CNCM I-2423CL0089 CNCM I-2423 type No Yes No Yes CNCM I-2425 CL0189 CNCM I-2425type Yes No No No

Sequences (5′-3′)

SEQ ID No. 1 S. thermophilus DSMZ-18344 CRISPR1 sequence leader sequenceactatgtgggtataaaaacatcaaaatttcatttgag SEQ ID No. 2 S.thermophilus DSMZ-18344CRISPR1 spacer (1) aatatctacaggtcactacaaagctacgctSEQ ID No. 3 S. thermophilus DSMZ-18344 CRISPR1 spacer (2)gttggggtgtgtttgtaacggcgtatgcta SEQ ID No. 4 S. thermophilus DSMZ-18344CRISPR1 spacer (3) tcaatcaggtgacggtgatgcttatattaa SEQ ID No. 5 S.thermophilus DSMZ-18344 CRISPR1 spacer (4)catacatgatagtttgtcaacacttttgat SEQ ID No. 6 S. thermophilus DSMZ-18344CRISPR1 spacer (5) tcagcatttggtttacatgacccacgtctg SEQ ID No. 7 S.thermophilus DSMZ-18344 CRISPR1 spacer (6)caatcaacaggtttgactgattataacggt SEQ ID No. 8 S. thermophilus DSMZ-18344CRISPR1 spacer (7) tagctacacatgaattttattacaatggtg SEQ ID No. 9 S.thermophilus DSMZ-18344 CRISPR1 spacer (8)ccgttcttcaaacgttaaattccaaggtgt SEQ ID No. 10 S. thermophilus DSMZ-18344CRISPR1 spacer (9) gctgcgattatgacaatgctgtctgtaagg SEQ ID No. 11 S.thermophilus DSMZ-18344 CRISPR1 spacer (10)gaagaatttattaataaagatggttctgct SEQ ID No. 12 S.thermophilus DSMZ-18344CRISPR1 spacer (11)aggcagaaaagaagtattttggtaagtatg SEQ ID No. 13 S. thermophilus DSMZ-18344CRISPR1 spacer (12) aaatggtttatcgacaagaaaatgaagct SEQ ID No. 14 S.thermophilus DSMZ-18344 CRISPR1 spacer (13)ccaaatttgcattatacaaaacgctccttc SEQ ID No. 15 S. thermophilus DSMZ-18344CRISPR1 spacer (14) atcctaactgctttgctaactacatcatgg SEQ ID No. 16 S.thermophilus DSMZ-18344CRISPR1 spacer (15)atcctaactgctttgctgactacatcatgg SEQ ID No. 17 S. thermophilus DSMZ-18344CRISPR1 spacer (16) taacaagataagattagtcgtcttctacat SEQ ID No. 18 S.thermophilus DSMZ-18344 CRISPR1 sequence trailer sequencettgattcaacataaaaagccagttcaattgaacttggcttt SEQ ID No. 19 S.thermophilus DSMZ-18344 CRISPR1 sequenceactatgtgggtataaaaacatcaaaatttcatttgaggtttttgtactctcaagatttaagtaactgtacaacaatatctacaggtcactacaaagctacgctgtttttgtactctcaagatttaagtaactgtacaacgttggggtgtgtttgtaacggcgtatgctagtttttgtactctcaagatttaagtaactgtacaactcaatcaggtgacggtgatgcttatattaagtttttgtactctcaagatttaagtaactgtacaaccatacatgatagtttgtcaacacttttgatgtttttgtactctcaagatttaagtaactgtacaactcagcatttggtttacatgacccacgtctggtttttgtactctcaagatttaagtaactgtacaaccaatcaacaggtttgactgattataacggtgtttttgtactctcaagatttaagtaactgtacaactagctacacatgaattttattacaatggtggtttttgtactctcaagatttaagtaactgtacaacccgttcttcaaacgttaaattccaaggtgtgtttttgtactctcaagatttaagtaactgtacaacgctgcgattatgacaatgctgtctgtaagggtttttgtactctcaagatttaagtaactgtacaacgaagaatttattaataaagatggttctgctgtttttgtactctcaagatttaagtaactgtacaacaggcagaaaagaagtattttggtaagtatggtttttgtactctcaagatttaagtaactgtacaacaaatggtttatcgacaagaaaatgaagctgtttttgtactctcaagatttaagtaactgtacaacccaaatttgcattatacaaaacgctccttcgtttttgtactctcaagatttaagtaactgtacaacatcctaactgctttgctaactacatcatgggtttttgtactctcaagatttaagtaactgtacaacatcctaactgctttgctgactacatcatgggtttttgtactctcaagatttaagtaactgtacaactaacaagataagattagtcgtcttctacatgtttttgtactctcaagatttaagtaactgtacagtttgattcaacataaaaagccag ttcaattgaacttggctttSEQ ID No. 20 S. thermophilus DSMZ-18344 BPS gene clustergctgagccagcttactagcgtacaggcacctactaaggttgataagaacaatatcgaggtcttgatgtcagctctcaaaaaagataaaaaagttgatgttaaagttgatgatgttgcttcatatcaagaagcttatgataatctcaagtctggcaaatctaaagctatggtcttgagtggctcttatgctagcctattagagtctgtcaatagtaaccttgcttcaaatctaaaaacaatttatacttataaaattaaaaagaagaataacaactctgcaaaccaagtagattcaaaagtcttcaatatttatattagtggtattgatacctacggttcgatttcaacagtgtcacgttcagatgtcaatattattatgacagtaaacatgaatacacataagattctcttgacgactactccacgtgatgcatacgttaagattcctggtggtggggcaaaccagtatgataaattaacccacgcaggtatttatggtgttgaaacatctgaacaaactctggaagatctatatggtactaagattgattactatgcacgaattaacttcacatctttccttaagttgattgaccaacttggtggtgtgacagtccataatgatcaagctttcacaagtcttcatgggaagtttgatttcccagttggagatatccaaatgaattcagagcaagcacttggatttgttcgtgaacgctatagtttagatggcggagataatgaccgtggtaaaaaccaggagaaagtcatttctgcgattgtaaacaagttggcttctctaaagtctgtatcaaactttacttcaatcgttaataatctccaagactctgttcagacaaatatttctttggataccattaatgctttggctaatacacaacttgattcaggctctaaatttacagtaacgtctcaagcagtaactggtacaggttcaaccggacaattgacctcttatgcgatgccaaattctagtctttacatgatgaaactagataattcgagtgtggcaagtgcctctcaagctatcaaaaatctgatggaggaaaaataagtgattgacgttcactcacatattgtttttgatgttgatgatggtcctaaaactttagaagaaagtttagacctcattggtgaaagttatgcccagggggtacgtaagattgtttcaacatcccatcgtcgtaaggggatgtttgagactccagaggataaaatttttgccaacttttctaaggtaaaagcagaagcagaagcactttatccagacttaactatttattatggaggtgaactttattacaccctagacattgtggagaaacttgaaaagaatctcattccgcgcatgcacaacactcaatttgctttgattgagtttagtgctcgcacatcttggaaagaaattcatagtgggcttagtaatgttttgagagcgggggtaacgcctattgttgctcatattgagcgctatgatgccctcgaagaaaatgctgatcgtgttagagaaattatcaatatgggctgctatactcaagtcaatagctcacatgtcctcaaaccaaagctctttggagataaagaaaaagtaagaaagaaacgtgttcgctttttcttggagaaaaatttggttcatatggttgctagcgacatgcataatcttgggccgagaccaccatttatgaaagatgcttatgaaattgttaaaaagaactacggctccaaacgtgctaagaatctttttattgaaaatcccaaaacattactagaaaatcaatatttataggagatattatgaatcaagataacactaaaagtgatgaaatcgacgtactagcattgctacataaactttggacgaagaagcttttgattcttttcacagctttttatttcgctgctttcagtttcttaggtacttatttctttatccaaccaacatatacatcaacaacgcttatctatgttgttaatcaggcaacagataataataatctttctgctcaagatttgcaagctggtacctatttggcaaatgactataaagagattattacatcaaatgatgtattatcagaagttattaaagatgaaaaattgaatttgagtgaggcagaactgtctaaaatggtttcagttaatattcctactgatactcgtcttatttcaatttctgttaatgctaaaactggtcaagatgcgcaaacacttgctaataaggttcgtgaagttgcttcaaaaaaaatcaagaaggtgacaaaagttgaagatttcacaatgctcgaagaagctaaattgccagagtcaccatcttcaccaaatatcaaacttaatgtgcttcttggggcagtgcttggaggattccttgcagtggttggtgtattggtacgtgaaatcctagatgatcgtgttcgccgtccagaagatgtggaagatgcccttggaatggcacttcttggaattgtccctgatacagataaaatttaaggagaagaaatgcctctattaaagttagtaaaatctaaagtaaactttgccaaacaaacagaagagtattacaatgccattcgcacaaatattcaattttctggtgctcagattaaagtgattgcgattagctctgttgaagctggtgaaggaaaatcaacgacatctcttaacttggcgatttcatttgctagtgttgggctccgaacacttctgattgatgctgatactcgtaattctgttttttcaggtacatttaaatcaaatgagccttataaaggtctttcaaattttctttcaggaaatgccgatctaaatgaaacgatttgccaaactgatatttctggtttggatgttattgcatctggtcctgttccacctaatccaacaagtcttttgcaaaatgacaattttagacatttgatggaagttgctcgtagtcgttatgattatgtcatcatcgatacaccaccagttggtttggttattgatgcagttattattgcccatcaggctgatgccagtcttttggttacagcagctgggaaaatcaaacgtcgtttcgtaactaaggccgtcgaacaattggaacaaagtggttctcagttcttaggtgtcgtccttaataaagttgacatgacagttgataaatatggatcatatggttcttacggatcatatggttcttacggatcatatggtgagtacaggaaaaaaacagaccaaactgaaggtcattcaagagcacatcgtcgtagaaaaggatagcattaatggggatgatgcggctccttataccttaacagattaaaaaggggtttagagtgaaagaaaaacaagaaattcgtcgcattgaaattggtattatacagttggttgtggttgttttcgcagccatggtagctagtaaaataccatatacagagattacccaaggaagtattgtccttttaggtgtcgtacatgtagtgtcttactatatcagtagttattatgaaaatcttaagtatagaggctacttggatgaactcattgcaactgtcaaatattgtttcatatttgctctaattgcaacatttctctcgttttttgcagatggaagtttttcaatctcacgtcgcggacttctttacgtcaccatgatttcaggtgttctcttatacgttacaaatactgttcttaagtatttccgctcatctatttatacacgtcgtaaaagtaacaagaatattctcttgatttctgatcaggcacgtcttgataatgttttgtctcgtatgaaagacaatatggatggtaggattacagcagtttgtgtcttggataatccttattttactgatccatttatcaagagtgttaaacctgaaaatttgattgaatatgcgacacactcagtagtagaccaagttttgattaatctgccaagtgggcagtataagatttgggattatgcatcaccttttgagatcatgggaattccagtttctattaatttgaatgcccttgaatttatgagtcaaggtgaaaaacgtattcaacaattgggtcctttcaaagttgttacgttttcaacgcaattttatagctatggagatatcttggcgaaacgtttcctcgatatctgtggagccctagttggtttggtgctctgtgggattgttggaatcttcctttatccacttattcgtaaggatggtgggccagccatttttgctcaagaccgtgtgggagaaaatggacgtatctttaagttttataaattccgttctatgtgtgttgatgcggaagaaatcaagaagaatttgatggcacagaatcaaatgtctggtggtatgtttaagatggacaatgatccacgtattacaaaaattggacgtttcattcgtaaaacaagtcttgatgaacttccacaattttggaatgtcctaaaaggtgatatgagcttggttgggacacgtcctccaacagttgatgagtatgaaaaatatacacctgaacagaaacgtcgtttaagttttaaacctggtatcactggtctttggcaagtaagcggtcgaagtgaaattactgattttgatgaagttgtaaaactagacgttgcttatttggacggatggacaatctggcgtgatatcaaaatcttattgaaaacaattaaagtagtagtaatgaaggatggagcaaagtgatggctttcaccatttcttttaatggtgattaaatgacaaaaacagtttatatcgttggttctaaggggattccagcaaaatatggtggatttgagacctttgttgagaagttgacagagttccaacaagacaaagatatccaatattatgtagcttgtatgcgggaaaactctgcaaaatcagacattacagcagatgattttcaaacttcgcaacagaaccctaaaaagaactccctaacggtcgtggctactttgtttagtctaaacactttgaatagtcctacaagctcatagtttcccttttattagttggtccaaggccaattctattttttgaagcgaaagaatatggggagcgccttccttatttactgatatgtaaacctggaattactggttattggacgacacatggtcgaagtaaagttctttttcctcaacgagcagatttagaactctattatctccaatattacagcaccaagaacgacatcaagcttctaatacgtacaatttcacaaatcattaacggattggacgcttactaaaaaattaatgaaaaaatatttgaaatcataactcgaaaaatattaaaagattagatatgtatcataaaacccgaattgctagttaatttcattggaaaataaataagtcgtgctatcctaatcttaaaccactaagcattagaaagcgcacgacttatatgacttataatagcacacttccaaaagtttttgtttatttactgacaaccattgagacgctttatcaaacgagtgttccccttgaggttcaaaaccgaaagaacgtccatctcgcaacatcagattgcttagttatcgcttgttacctatggggcgtactgcattttagtgaaacgcttaaagcaaagcaccaattggctcaaagtttatttcctaatttcctagaatattctcactttgtccgccgttgtaatgccctcttaccgagtatccaagtcattcgccaagcactcgtatttaaagaggttgaaggaattagtgtatccattattgacagcttccccattcctttgtgtcagtctattcgtaatttcagaagcaaagttcttggagattatgcaaatgttggctacaatgctacaaagggacagtacttctatggatgtaaatgtcatgctttagtcagtgaatcaggctatgtcatagactacacaattactcctgcttcaatggctgatagttcaatgaccgaggaagtgttgagtcaatttgggacaccaacagtccttggagatatgggatatttaggtcagtcactgcatgataggctggaattaaaaggaattgatctaattacacctgtcaggaagaacatgaagcaaaagaaaattcttttccctaatttttcaaaacgtagaaaagtgattgagcgagttttctcttttttgacaaatctaggagctgagcgttgtaaaagtcgttcgcctcaaggttttcaattgaaattagagatgatacttttagcgtattctttactgttaaaatcagctaaatcactggaaccagagactttaagatattctatcgggtatcaagtcatggctaaataatcaactagcaattcgggtatcataaaggagtgatttaatgaaaaaaattacaatagcagttgcaacgcataaaaaatatcaaatgccaaaagataatatttatctaccaattgaatgtggagcagttttaagaaaaaatcacctagactatattgctgatgatagtggagataatatttctgaaaaaaacaagaattattcagagttaacagcactatattggttatggaaaaataatgattctgagtataaaggattagcacactatagacgtcatttttcagataaaaaggtgagtattttttctacaggtaattttgataatatacttgataggacggtacttgaggaacatttagagaagtttgatattatacttcccaagcttcgacattactatattgaaacaatagaatctcactataaacatacgcattttgaaaaagatttattagcaacagaagaaataattaaaaaactatatcctgactatcttgatttttattatagtgcactaaaaagaaaatctgctcatatgtttaatatgtttattatgaaagataaatatttcaataattattgtgaatggttattttcgattctttttgaattagaaaaagtactagatatttcagaatattctccctttcatgcaagagtatttggtcgtgtgagtgaaattttattagatgtatggattttcaagaataatttaaatttcactgaaattccagttatgtttatggaaaagcaaaattggtgggataaatctaaaagatttatttctgcaaagcttttcaacaaaaaatattattagactaggagaaataaattgcttacaatcggaataattttaataatttttatgactattttcgattattatatacataaaacagtattttctccggtctttatgtttaattcactctttttattaataatatctctttcttctatgaggttatataatttgagagaatattctatcaaatcaatagaagtaattgtgttagggatgatattcttctctttaggagtattttgtactcgtattgtttctcatgaatttttaaaaaatcaaaataatgttattaattacgatgataatttaaatgtaaattggacttttttaaaaattcttttgatagttgtaaccacaggaaacgtattctctattattttttccttgaaattccttttaggaggaggttcatacttagaattgagaaatatgatattgggatataatggagctgaaccacttattacgaatcctctcgtaaatatattaacaagatatatatcgggaccagggttgactgctttgatcccattttctattttttttctaattaggaaaaaaaacattaaattttccttaattattttattgaatcttgttttggcaacattatcatccggtggtagaattttacttgtatatactattattcaattgtttataggattatcttattcaaaaaaaaatataccaaaaaaaattaagaaagtagtcataatatcaagtattatattttttatatctataattgtcttatctaacatcagaagttctaacagtatatatagagcgttttatgcatacttttcgggccctgtagttcttttatctacttggatgactgatgttgatacttataatattcattcacatggattaggatttatttatcccatcacatatctattaaattcattttgtaatttaataggaattcctaactcgatgttggctaatgttgtcatgtggcaaggaatgcctcagaatgattgggtaggcgtattccctaatcaatcgatgaacgcttttagtacacttttctattttttctataaagattttcgagaatttggagttgcttgcttttctttcctttttgggagtatttgtggttttatttattttaaagcgtttatcgaaagaaaaagtaaatatctagtctattatttattaggggtacaggcaattatcggatcttttattatttggcaattggggagtactgcgtttttcttaagtattgtatttacaatattaagtctgaaatcaaagaaatcataactatagaaaaggagataaaatatgacaatcagcatagtaatcccagtttataatgttcaagattacataaaaaagtgtctagattctatattaagccagacattttcagatttagaaattattcttgttgatgatggttctactgacttgagtggaagaatttgtgattattattccgaaaatgataaacgtattaaagtaatccacacagcaaatgggggacagtcggaagcaaggaacgttggaatcaaaaatgccacatcagaatggataacatttattgattctgatgactacgtttcttctgattatatagagtatttatataatttgattcaagtacacaatgcagatatttcaatagctagttttacctatatcacacctaaaaagataattaagcacggtaacggtgaagtagctcttatggatgcaaaaactgcaattcggagaatgttactgaatgaaggtttcgatatgggagtttgggggaaaatgtatcgaacggagtattttaataaatataaattcgtttcaggaaaactatttgaagattctttaattacataccagatattttcagaagcttcaacaattgtttttggagcaaaggatatttatttttatgttaacaggaaaaattctactgttaatggtacttttaatataaaaaagtttgatcttattgaaatgaatgaagaagcaaataagtttattaaacataaatttccagatctttcatctgaagcacatcgtcgaatgatatgggcatattttagtacactaaatcaagttttatcatcaactaatgaacacgatattgatttatatgcgccacaattagtagcttatctccttaaacaggataaattcataaaaaggaatacttttattcccaaaagagataagattgcattttttattttaaaaaattttggtttaaagacatatcgtaatgtttggaatttatatttaaaaatgacaagataaaaacaataatgaaagataaaaaataatgaaaactgctacaattactttacattcagcacataataatggatctatcttttctacagtcatttgctttgcagagaaagataatatctatgggatatgataacgaaattataaattatattccactcaaattgctcgtagttttaagaaccaagtgcaaaagattattaaggttaacaacgttacgattgttgctacggccgcaacgccgaagaagccgctgaatacgttgattgggctagttgtcggcttgctataggatttgtttatgcagcgattcggatgctcacggatcgccgcgttcacgaagctgatttcttaactgatgaattaggattgactagtttaggcttggttaaccatcaacatcaccattcaatgaagaaacaggccttgaatctgaacggtggctatcatacgcataacgatcaaacatcttcacaagcgatgaaacgagtttaggagggtgctagatgtttaaacgtaaagaaaagaatataacgactacggcaccaattaatctcaccacgattaatgaacccatgtcggtcattactgagcagattaaaacaattcgaaccaatatcaatt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All publications mentioned in the above specification are hereinincorporated by reference. Various modifications and variations of thedescribed methods and system of the present invention will be apparentto those skilled in the art without departing from the scope and spiritof the present invention. Although the present invention has beendescribed in connection with specific preferred embodiments, it shouldbe understood that the invention as claimed should not be unduly limitedto such specific embodiments. Indeed, various modifications of thedescribed modes for carrying out the invention which are obvious tothose skilled in biochemistry, microbiology and molecular biology orrelated fields are intended to be within the scope of the followingclaims.

1. A fast acidifying lactic acid bacterium that generates a viscosity infermented milk greater than about 62 Pa·s after 14 days of storage at 6°C.
 2. The lactic acid bacterium according to claim 1, wherein saidbacterium is phage resistant.
 3. The lactic acid bacterium according toclaim 1, wherein said bacterium is selected from the group consisting ofStreptococcus, Lactococcus, Lactobacillus, Leuconostoc, Pediococcus andBifidobacterium.
 4. The lactic acid bacterium according to claim 1,wherein said bacterium is Streptococcus thermophilus.
 5. The lactic acidbacterium according to claim 4, or a mutant thereof and/or a variantthereof, wherein said Streptococcus thermophilus belongs to the geneticcluster CLO189.
 6. The lactic acid bacterium according to claim 1, or amutant thereof and/or a variant thereof, wherein said bacteriumcomprises the sequence set forth in SEQ ID No.
 20. 7. A lactic acidbacterium or a mutant thereof and/or a variant thereof, comprising thesequence set forth in SEQ ID No. 19 or a homologue thereof with at least75% identity thereto.
 8. An isolated Streptococcus thermophilus straindeposited at DSMZ (Deutsche Sammlung von Mikroorganismen undZellkulturen GmbH, Mascheroder Weg 1 b, D-38124 Braunschweig) underdeposit number 18344 on 14 Jun. 2006 or a mutant thereof and/or avariant thereof.
 9. A cell culture comprising the lactic acid bacteriumaccording to claim
 1. 10. The cell culture according to claim 9, whereinsaid cell culture is a starter culture, a probiotic culture or a dietarysupplement.
 11. The cell culture according to claim 9, wherein saidculture comprises one or more further lactic acid bacteria selected fromthe genera consisting of Streptococcus, Lactococcus, Lactobacillus,Leuconostoc, Pediococcus and Bifidobacterium.
 12. The cell cultureaccording to claim 9, wherein said culture comprises one or more furtherlactic acid bacteria selected from the species consisting ofLactobacillus delbrueckii subsp. bulgaricus, Lactobacillus acidophilus,Lactobacillus casei and/or Bifidobacterium.
 13. A food, food additive,feed, nutritional supplement, or probiotic supplement comprising thelactic acid bacterium according to claim
 1. 14. A food, food additive,feed, nutritional supplement, or probiotic supplement according to claim13, wherein the food, food additive, feed, nutritional supplement, orprobiotic supplement is a dairy, meat or cereal food, food additive,feed, nutritional supplement, or probiotic supplement
 15. A dairy food,food additive, feed, nutritional supplement, or probiotic supplementaccording to claim 14, wherein the dairy food, food additive, feed,nutritional supplement, or probiotic supplement is a fermented milk,yoghurt, cream, matured cream, cheese, fromage frais, a milk beverage, aprocessed cheese, a cream dessert, a cottage cheese or infant milk. 16.A food, food additive, feed, nutritional supplement, or probioticsupplement according to claim 15, wherein the milk comprises milk ofanimal and/or plant origin.
 17. A method for preparing a food, foodadditive, feed, nutritional supplement, or probiotic supplementcomprising the step of adding the lactic acid bacterium according toclaim
 1. 18. The method according to claim 17, wherein said food, foodadditive, feed, nutritional supplement, or probiotic supplementcomprises or consists of a fermented food, food additive, feed,nutritional supplement, or probiotic supplement.
 19. The methodaccording to claim 17, wherein said food, food additive, feed,nutritional supplement, or probiotic supplement comprises or consists ofa dairy food, food additive, feed, nutritional supplement, or probioticsupplement.
 20. A food, food additive, feed, nutritional supplement, orprobiotic supplement obtained or obtainable by the method of claim 17.21. Use of the lactic acid bacterium according to claim 1 for preparinga food, food additive, feed, nutritional supplement, or probioticsupplement.
 22. A method for modulating or modifying the viscosity of afood, food additive, feed, nutritional supplement, or probioticsupplement, comprising adding the lactic acid bacterium according toclaim
 1. 23. A food, food additive, feed, nutritional supplement, orprobiotic supplement obtained or obtainable by the method of claim 22.24. Use of the strain according to claim 8 for modifying the viscosityof a food, food additive, feed, nutritional supplement, or probioticsupplement.
 25. A method for identifying a bacterium belonging to thegenus Streptococcus comprising the step of screening the bacterium forthe sequence set forth in SEQ ID No. 19 or a homologue thereof with atleast 75% identity thereto.
 26. A method for identifying a bacteriumbelonging to the genus Streptococcus comprising the step of amplifyingthe CRISPR locus of a bacterium using at least one forward and at leastone reverse oligonucleotide primer, wherein each of the primers flankopposite sides of one or more CRISPR spacers that are absent inStreptococcus thermophilius DSMZ-18344.
 27. A method according to claim26, wherein the forward oligonucleotide primer hybridises to SEQ ID No.1 and the reverse oligonucleotide primer hybridises to any of SEQ ID No.2, SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, SEQ ID No. 7,SEQ ID No. 8, SEQ ID No. 9, SEQ ID No. 10, SEQ ID No. 11, SEQ ID No. 12,SEQ ID No. 13, SEQ ID No. 14, SEQ ID No. 15, SEQ ID No. 16 and/or SEQ IDNo.
 17. 28. A method according to claim 26, wherein the forwardoligonucleotide primer hybridises to any of SEQ ID No. 2, SEQ ID No. 3,SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, SEQ ID No. 7 and/or SEQ ID No.8 and a reverse oligonucleotide primer hybridises to any of SEQ ID No.9, SEQ ID No. 10, SEQ ID No. 11, SEQ ID No. 12, SEQ ID No. 13, SEQ IDNo. 14, SEQ ID No. 15, SEQ ID No. 16 and/or SEQ ID No.
 17. 29. A methodaccording to claim 26, wherein the forward oligonucleotide primerhybridises to any of SEQ ID No. 2, SEQ ID No. 3, SEQ ID No. 4, SEQ IDNo. 5, SEQ ID No. 6, SEQ ID No. 7 and/or SEQ ID No. 8 and the reverseoligonucleotide primer hybridises to SEQ ID No.
 18. 30. A methodaccording to claim 26, wherein the forward oligonucleotide primerhybridises to any of SEQ ID No. 9, SEQ ID No. 10, SEQ ID No. 11, SEQ IDNo. 12, SEQ ID No. 13, SEQ ID No. 14, SEQ ID No. 15, SEQ ID No. 16and/or SEQ ID No. 17 and the reverse oligonucleotide primer hybridisesto SEQ ID No.
 18. 31. A method according to claim 25, wherein thebacterium belonging to the genus Streptococcus is Streptococcusthermophilus.
 32. A method according to claim 31, wherein theStreptococcus thermophilus strain belongs to the genetic cluster CLO189.33. A method according to claim 31, wherein the Streptococcusthermophilus strain has substantially the same characteristics as theStreptococcus thermophilus strain deposited at DSMZ (Deutsche Sammlungvon Mikroorganismen und Zellkulturen GmbH, Mascheroder Weg 1 b, D-38124Braunschweig) under deposit number 18344 on 14 Jun.
 2006. 34. A methodaccording to claim 31, wherein the Streptococcus thermophilus strain isthe same as the Streptococcus thermophilus strain deposited at DSMZ(Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH,Mascheroder Weg 1 b, D-38124 Braunschweig) under deposit number 18344 on14 Jun.
 2006. 35. A bacterium belonging to the genus Streptococcus thatis identified or identifiable by the method according to claim
 25. 36. Anucleotide sequence comprising the sequence set forth in SEQ ID No. 19or a homologue thereof with at least 75% identity thereto.
 37. Anucleotide sequence complementary to the nucleotide sequence of claim36.
 38. A construct or a vector comprising the nucleotide sequenceaccording to claim
 36. 39. A host cell comprising the construct or thevector according to claim
 38. 40. An oligonucleotide primer that iscapable of hybridising to the nucleotide sequence of claim
 36. 41. Useof an oligonucleotide primer according to claim 40 for identifying abacterium belonging to the genus Streptococcus.
 42. (canceled)